Canonical Allele Identifier: PA116600
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 4024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Arg725Trp
CA116598
NM_001079803.3:c.2173C>T