Canonical Allele Identifier: PA193561
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 185982
ClinVar RCV Id: RCV000165499 RCV000203957 RCV000759877 RCV002492662
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Ser346Trp
CA012006
NM_001128425.2:c.1037C>G