Canonical Allele Identifier: PA2827998905
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 921617
ClinVar RCV Id: RCV001181165

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2513Leu
CA16038090
NM_001354901.2:c.7538C>T