Allele Registry

Canonical Allele Identifier: PA098086

Gene: MMACHC HGNC NCBI

ClinVar RCV:

RCV000490478

ClinVar Variation:

203832

HGVS (amino-acid)	Matching Registered Transcripts
NP_056321.2:p.Arg206Trp	CA312738 NM_015506.3:c.616C>T