Canonical Allele Identifier: PA2826827385
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 928029
ClinVar RCV Id: RCV001191678

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280121.1:p.Thr348Ala
CA340132645
NM_001293192.2:c.1042A>G