Canonical Allele Identifier: PA913200893
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 627803

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Gly503Trp
CA340132324
NM_001128425.2:c.1507G>T