Canonical Allele Identifier: PA2826826745
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 918380
ClinVar RCV Id: RCV001175948

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280121.1:p.Ser139Ala
CA340134773
NM_001293192.2:c.415T>G