Canonical Allele Identifier: PA092059
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 5299
ClinVar RCV Id: RCV000005620
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036354.1:p.Gln411Arg
CA011596
NM_012222.3:c.1232A>G