Canonical Allele Identifier: PA658826234
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 550859
ClinVar RCV Id: RCV000665730

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Met427Thr
CA401365341
NM_000152.5:c.1280T>C