Canonical Allele Identifier: PA2741836358
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 2701377
ClinVar RCV Id: RCV003505763
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Gly429Ala
CA340132892
NM_001128425.2:c.1286G>C