Canonical Allele Identifier: PA2827996933
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 187282
ClinVar RCV Id: RCV000167000 RCV000455669 RCV000677738 RCV002260627 RCV001358361 RCV003975238 RCV003323298 RCV003743616 RCV003995547
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser1912Cys
CA010787
NM_001354901.2:c.5735C>G