Canonical Allele Identifier: PA169672
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 142884
ClinVar RCV Id: RCV000132344 RCV000198891 RCV001558131
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Gln498His
CA012950
NM_001128425.2:c.1494G>C
CA340132369
NM_001128425.2:c.1494G>T