Canonical Allele Identifier: PA2827983269
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1777096
ClinVar RCV Id: RCV002403589

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Leu507Ser
CA16024897
NM_001354900.2:c.1520T>C