Canonical Allele Identifier: PA916018765
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 142131

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280125.1:p.Met81Val
CA013944
NM_001293196.2:c.241A>G