Canonical Allele Identifier: PA2825644355
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1511850
ClinVar RCV Id: RCV003773417

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ala2483Ser
CA16037645
NM_001127511.3:c.7447G>T