Canonical Allele Identifier: PA186897
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 183896
ClinVar RCV Id: RCV000162761 RCV000230772 RCV000442590 RCV001353971 RCV003162684
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Arg109Trp
CA013370
NM_001128425.2:c.325C>T