Canonical Allele Identifier: PA913200882
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 628978

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Gln454Pro
CA056232
NM_001128425.2:c.1361A>C