Canonical Allele Identifier: PA2573184369
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_001161079.1:p.Ser29Pro
CA361805725
NM_001167607.3:c.85T>C