Canonical Allele Identifier: PA198638
Gene: MTHFR HGNC NCBI

Linked Data

ClinVar Variation Id: 187894
ClinVar RCV Id: RCV000167614
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005948.3:p.Tyr506Asp
CA198636
NM_005957.5:c.1516T>G