Canonical Allele Identifier: PA116592
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 4021
ClinVar RCV Id: RCV000004236 RCV000727662 RCV000780268
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Met318Thr
CA116590
NM_001079803.3:c.953T>C