Canonical Allele Identifier: PA2827986900
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_001341829.1:p.Gly1637Glu
CA16032340
NM_001354900.2:c.4910G>A
CA1573473273
NM_001354900.2:c.4910_4911delinsAA