Canonical Allele Identifier: PA2826826100
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_001280120.1:p.Thr466Ser
CA340132548
NM_001293191.2:c.1397C>G
CA340132551
NM_001293191.2:c.1396A>T