Canonical Allele Identifier: PA2825163186
Gene: GM2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1388998
ClinVar RCV Id: RCV001878113
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000396.2:p.Ser29Pro
CA361805725
NM_000405.5:c.85T>C