Canonical Allele Identifier: PA2826829764
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 142402
ClinVar RCV Id: RCV000131501 RCV001062564
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280125.1:p.Gly217Arg
CA011941
NM_001293196.2:c.649G>A
CA340133905
NM_001293196.2:c.649G>C