Canonical Allele Identifier: PA915964845
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 580157
ClinVar RCV Id: RCV000703619

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Phe728Leu
CA401370649
NM_001079804.3:c.2182T>C
CA401370654
NM_001079804.3:c.2184C>G
CA401370655
NM_001079804.3:c.2184C>A