Canonical Allele Identifier: PA915964563
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 284865
ClinVar RCV Id: RCV000343108

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Asp404Val
CA10604928
NM_001079804.3:c.1211A>T