Canonical Allele Identifier: PA2826823338
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 142812
ClinVar RCV Id: RCV000132238 RCV000195451 RCV000212698 RCV000656907 RCV001353576
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280119.1:p.Arg103Trp
CA013382
NM_001293190.2:c.307C>T