Canonical Allele Identifier: PA2828018850
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_001341835.1:p.Ser727Asn
CA348296
NM_001354906.2:c.2180G>A