Canonical Allele Identifier: PA2826829662
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 230638
ClinVar RCV Id: RCV000215490 RCV000704136 RCV001284023
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280125.1:p.Ser184Arg
CA059578
NM_001293196.2:c.552C>G
CA340134348
NM_001293196.2:c.552C>A
CA340134358
NM_001293196.2:c.550A>C