Canonical Allele Identifier: PA645453436
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 230077

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Ala399Ser
CA10577711
NM_001128425.2:c.1195G>T