Canonical Allele Identifier: PA2827999248
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2677396

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2615Pro
CA16038751
NM_001354901.2:c.7843T>C