Canonical Allele Identifier: PA2826829338
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1745522
ClinVar RCV Id: RCV002338158
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280125.1:p.Asn51Thr
CA340135839
NM_001293196.2:c.152A>C