Canonical Allele Identifier: PA2826247327
Gene: MTHFS HGNC NCBI

Linked Data

ClinVar Variation Id: 2038284
ClinVar RCV Id: RCV002890631

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186687.1:p.Thr145Ala
CA7690251
NM_001199758.1:c.433A>G