NG_011963.2:g.21351G>A

HGVS Expressions

  • NG_011963.2:g.21351G>A
Back to search Result
Genomic Location

chr13:30729828

CTGA Clinical Significance

Benign

Variant Type

Substitution

Epidemiology in the Arab World

View Map
© CAGS 2025. All rights reserved.