Canonical Allele Identifier: PA2826824338
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1172231
ClinVar RCV Id: RCV001525915

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280119.1:p.Val430Phe
CA340132802
NM_001293190.2:c.1288G>T