Canonical Allele Identifier: PA2826827169
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1011918
ClinVar RCV Id: RCV001309790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280121.1:p.Trp282Arg
CA340133144
NM_001293192.2:c.844T>A
CA340133145
NM_001293192.2:c.844T>C