Canonical Allele Identifier: PA287857
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 127833
ClinVar RCV Id: RCV000115751 RCV000212722 RCV000233496
ClinVar Variation Id: 492024
ClinVar RCV Id: RCV000584538 RCV001853927
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Met524Leu
CA011670
NM_001128425.2:c.1570A>T
CA340131758
NM_001128425.2:c.1570A>C