Canonical Allele Identifier: PA2829726161
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 182690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036354.1:p.Ala237Val
CA014186
NM_012222.3:c.710C>T