Canonical Allele Identifier: PA348298
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 220569
ClinVar RCV Id: RCV000204027 RCV001018168 RCV003997646
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser1010Asn
CA348296
NM_001127510.3:c.3029G>A