Canonical Allele Identifier: PA2826828986
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1771785
ClinVar RCV Id: RCV002389262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280124.1:p.Thr439Asn
CA340132649
NM_001293195.2:c.1316C>A