Canonical Allele Identifier: PA916040749
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482259
ClinVar RCV Id: RCV000567946 RCV004000946 RCV002528027 RCV003537105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Lys1911Glu
CA042579
NM_001354896.2:c.5731A>G