Canonical Allele Identifier: PA2825065763
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 661512
ClinVar RCV Id: RCV000818942

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Val480Ala
CA401366767
NM_000152.5:c.1439T>C