Canonical Allele Identifier: PA192158
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 185512
ClinVar RCV Id: RCV000164952 RCV000555612 RCV000612945 RCV001354534 RCV003151751 RCV003153444
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Arg97Gln
CA013305
NM_001128425.2:c.290G>A