Canonical Allele Identifier: PA2827556483
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 233334
ClinVar RCV Id: RCV000219640 RCV000470639 RCV001192932
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337579.1:p.Ala47Ser
CA10577730
NM_001350650.2:c.139G>T