Canonical Allele Identifier: PA2825015578
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1777096
ClinVar RCV Id: RCV002403589

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Leu548Ser
CA16024897
NM_000038.6:c.1643T>C