Canonical Allele Identifier: PA2827991421
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411556
ClinVar RCV Id: RCV000465724 RCV000572577 RCV000779741 RCV001357050 RCV003743727 RCV004001981
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Arg200Trp
CA049073
NM_001354901.2:c.598C>T