Canonical Allele Identifier: PA2825065701
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 2862966
ClinVar RCV Id: RCV003609110

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Pro457Ser
CA401366410
NM_000152.5:c.1369C>T