Canonical Allele Identifier: PA2826827569
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 819558
ClinVar Variation Id: 1332084
ClinVar RCV Id: RCV001804600

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280121.1:p.Met404Ile
CA340131745
NM_001293192.2:c.1212G>T
CA340131747
NM_001293192.2:c.1212G>C
CA340131749
NM_001293192.2:c.1212G>A