Canonical Allele Identifier: PA2829726910
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 967721
ClinVar Variation Id: 2567648
ClinVar RCV Id: RCV003278609

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036354.1:p.Thr480Ser
CA340132548
NM_012222.3:c.1439C>G
CA340132551
NM_012222.3:c.1438A>T