Canonical Allele Identifier: PA1139670556
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 842132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Arg168Trp
CA8814882
NM_001079804.3:c.502C>T