Canonical Allele Identifier: PA156792
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127315
ClinVar RCV Id: RCV000120028 RCV000115116 RCV000122796 RCV000501432 RCV002228340 RCV003477493 RCV003492450 RCV003743566
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala2286Val
CA012589
NM_000038.6:c.6857C>T