Canonical Allele Identifier: PA286622
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127301
ClinVar RCV Id: RCV000219975 RCV000410427 RCV000758730 RCV001355446 RCV003492449 RCV003952545 RCV003997220
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Glu1673Lys
CA009832
NM_000038.6:c.5017G>A