Canonical Allele Identifier: PA2825636259
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2677396

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser2674Pro
CA16038751
NM_001127510.3:c.8020T>C