Canonical Allele Identifier: PA916004121
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 657571
ClinVar RCV Id: RCV000814205
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036354.1:p.Gly25Ser
CA026524
NM_012222.3:c.73G>A