Canonical Allele Identifier: PA658672017
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 464695

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Gln478Arg
CA340132596
NM_001128425.2:c.1433A>G