Canonical Allele Identifier: PA116589
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 4020
ClinVar RCV Id: RCV000004235 RCV000078177 RCV000117106 RCV000531082 RCV002426487
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Asp91Asn
CA116586
NM_001079803.3:c.271G>A