Canonical Allele Identifier: PA916041554
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 647034
ClinVar RCV Id: RCV003653346

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser2599Gly
CA16038141
NM_001354896.2:c.7795A>G