Canonical Allele Identifier: PA916041652
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411376
ClinVar RCV Id: RCV000575522 RCV002230144 RCV004001927
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asp2681Gly
CA16038681
NM_001354896.2:c.8042A>G