Canonical Allele Identifier: PA645453973
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 418929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Thr539Ala
CA057086
NM_001128425.2:c.1615A>G