Canonical Allele Identifier: PA2580154546
Gene: GM2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2161013
ClinVar RCV Id: RCV003087830
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161079.1:p.Pro61Arg
CA3517888
NM_001167607.3:c.182C>G