Allele Registry

Canonical Allele Identifier: PA098057

Gene: MMACHC HGNC NCBI

ClinVar RCV:

RCV001004154

ClinVar Variation:

813351

HGVS (amino-acid)	Matching Registered Transcripts
NP_056321.2:p.Arg161Gly	CA340133167 NM_015506.3:c.481C>G