Canonical Allele Identifier: PA891860389
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 567406
ClinVar RCV Id: RCV000687481

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Leu401Gln
CA340133149
NM_001128425.2:c.1202T>A