Canonical Allele Identifier: PA2828048608
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1482706
ClinVar RCV Id: RCV003773166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser2468Pro
CA16038233
NM_001354904.2:c.7402T>C