Canonical Allele Identifier: PA2825428804
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_001041637.1:p.Thr456Ser
CA340132548
NM_001048172.1:c.1367C>G
CA340132551
NM_001048172.1:c.1366A>T