Canonical Allele Identifier: PA2825024682
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470103

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser2556Leu
CA048890
NM_000038.6:c.7667C>T