Canonical Allele Identifier: PA2826827341
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1770733
ClinVar RCV Id: RCV002383390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280121.1:p.Tyr333Ser
CA340132739
NM_001293192.2:c.998A>C