Canonical Allele Identifier: PA2829726786
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1172231
ClinVar RCV Id: RCV001525915
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036354.1:p.Val440Phe
CA340132802
NM_012222.3:c.1318G>T