Canonical Allele Identifier: PA2828049118
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2677396

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser2548Pro
CA16038751
NM_001354904.2:c.7642T>C