Canonical Allele Identifier: PA211338
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135716
ClinVar RCV Id: RCV000131625 RCV000148359 RCV000211933 RCV001719892 RCV003905173 RCV003743581 RCV003153405 RCV000987581 RCV001151806
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ile2329Val
CA012738
NM_000038.6:c.6985A>G