Canonical Allele Identifier: PA2826823122
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 41760

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280119.1:p.Val22Met
CA011797
NM_001293190.2:c.64G>A