Allele Registry

Canonical Allele Identifier: PA083052

Gene: HNMT HGNC NCBI

ClinVar RCV:

RCV000203518

ClinVar Variation:

219125

HGVS (amino-acid)	Matching Registered Transcripts
NP_008826.1:p.Gly60Asp	CA280933 NM_006895.3:c.179G>A