Canonical Allele Identifier: PA2827556621
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 2836859
ClinVar RCV Id: RCV003613997

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337579.1:p.Asp93Tyr
CA340134910
NM_001350650.2:c.277G>T