Canonical Allele Identifier: PA2826825002
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1735139
ClinVar RCV Id: RCV002355232

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280120.1:p.Ala110Val
CA340136244
NM_001293191.2:c.329C>T