Canonical Allele Identifier: PA2825065667
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 2139577
ClinVar RCV Id: RCV003052669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Met439Val
CA294892660
NM_000152.5:c.1315A>G