Canonical Allele Identifier: PA2827022628
Gene: GNMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1400150
ClinVar RCV Id: RCV001932648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305794.1:p.Asp37Glu
CA364143368
NM_001318865.2:c.111C>A
CA364143369
NM_001318865.2:c.111C>G