Allele Registry

Canonical Allele Identifier: PA083279

Gene: HNMT HGNC NCBI

ClinVar RCV:

RCV000203542

ClinVar Variation:

219126

HGVS (amino-acid)	Matching Registered Transcripts
NP_008826.1:p.Leu208Pro	CA347928 NM_006895.3:c.623T>C