Canonical Allele Identifier: PA2827556698
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 918380
ClinVar RCV Id: RCV001175948

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337579.1:p.Ser116Ala
CA340134773
NM_001350650.2:c.346T>G