Canonical Allele Identifier: PA1139671157
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 857246
ClinVar RCV Id: RCV001062884

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Met439Ile
CA294892670
NM_001079804.3:c.1317G>C
CA401365414
NM_001079804.3:c.1317G>A
CA401365415
NM_001079804.3:c.1317G>T