Canonical Allele Identifier: PA658830498
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 41760

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036354.1:p.Val22Met
CA011797
NM_012222.3:c.64G>A