Canonical Allele Identifier: PA2828015983
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1777096
ClinVar RCV Id: RCV002403589

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Leu265Ser
CA16024897
NM_001354906.2:c.794T>C