Canonical Allele Identifier: PA2826823696
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 2836859
ClinVar RCV Id: RCV003613997

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280119.1:p.Asp223Tyr
CA340134910
NM_001293190.2:c.667G>T