Canonical Allele Identifier: PA2828048527
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1297699
ClinVar RCV Id: RCV001723464

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser2460Asn
CA16038179
NM_001354904.2:c.7379G>A