Canonical Allele Identifier: PA168464
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 135986
ClinVar RCV Id: RCV000123149 RCV000131617 RCV000609799 RCV000759161
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Asp105Asn
CA013355
NM_001128425.2:c.313G>A