Canonical Allele Identifier: PA2826823786
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 862299
ClinVar RCV Id: RCV001068994

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280119.1:p.Trp250Ser
CA340134746
NM_001293190.2:c.749G>C