Canonical Allele Identifier: PA1139728199
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 918410
ClinVar RCV Id: RCV001175980
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337580.1:p.Ala97Pro
CA340134873
NM_001350651.2:c.289G>C