Canonical Allele Identifier: PA2826824733
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1046297
ClinVar RCV Id: RCV001350839

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280120.1:p.Ala17Asp
CA340137141
NM_001293191.2:c.50C>A