Canonical Allele Identifier: PA2828027902
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482462
ClinVar RCV Id: RCV000572004

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Lys2129Asn
CA16037092
NM_001354906.2:c.6387A>C
CA16037093
NM_001354906.2:c.6387A>T