Canonical Allele Identifier: PA2827955119
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_001341826.1:p.Arg269Trp
CA049073
NM_001354897.2:c.805C>T