Canonical Allele Identifier: PA170992
Gene: MTHFR HGNC NCBI

Linked Data

ClinVar Variation Id: 3520
ClinVar Variation Id: 2194685
ClinVar RCV Id: RCV002647482

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005948.3:p.Ala222Val
CA170990
NM_005957.5:c.665C>T
CA2580060904
NM_005957.5:c.665_666delinsTT