Canonical Allele Identifier: PA2827996061
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1474360
ClinVar RCV Id: RCV003773096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser1647Leu
CA16032517
NM_001354901.2:c.4940C>T