Canonical Allele Identifier: PA913200288
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 630899
ClinVar RCV Id: RCV000776918 RCV003768411
ClinVar Variation Id: 1047386
ClinVar RCV Id: RCV002242436 RCV003169750
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gly1678Glu
CA16032340
NM_001127510.3:c.5033G>A
CA1573473273
NM_001127510.3:c.5033_5034delinsAA