Canonical Allele Identifier: PA1139672070
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 857904
ClinVar RCV Id: RCV001063671

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Leu769Ser
CA401324904
NM_001079804.3:c.2306T>C