Canonical Allele Identifier: PA915964587
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 550859
ClinVar RCV Id: RCV000665730

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Met427Thr
CA401365341
NM_001079804.3:c.1280T>C