Canonical Allele Identifier: PA2825462909
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 857904
ClinVar RCV Id: RCV001063671

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Leu769Ser
CA401324904
NM_001079803.3:c.2306T>C