Canonical Allele Identifier: PA915964632
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 497673

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Asp459His
CA294893978
NM_001079804.3:c.1375G>C