Canonical Allele Identifier: PA916039765
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184580
ClinVar RCV Id: RCV000163857 RCV000197204 RCV000236573 RCV001193496 RCV003534432 RCV003995289
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asn759Ser
CA007300
NM_001354896.2:c.2276A>G