Canonical Allele Identifier: PA2827556629
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 419292
ClinVar RCV Id: RCV000479523 RCV000574246 RCV001851159
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337579.1:p.Asn95Thr
CA16617163
NM_001350650.2:c.284A>C