Canonical Allele Identifier: PA2827998413
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2362Leu
CA047405
NM_001354901.2:c.7085C>T