Canonical Allele Identifier: PA2827558488
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1018594
ClinVar RCV Id: RCV001317921
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337580.1:p.His305Tyr
CA340132773
NM_001350651.2:c.913C>T