Canonical Allele Identifier: PA2825431871
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 140816
ClinVar RCV Id: RCV000129005 RCV000410796 RCV000587968 RCV004525829
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041639.1:p.His407Tyr
CA012561
NM_001048174.1:c.1219C>T