Canonical Allele Identifier: PA2825430387
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 819183
ClinVar RCV Id: RCV001011521
ClinVar Variation Id: 933734

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041638.1:p.Trp447Arg
CA340132615
NM_001048173.1:c.1339T>C
CA340132616
NM_001048173.1:c.1339T>A