Canonical Allele Identifier: PA2828030405
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser2516Pro
CA16039553
NM_001354906.2:c.7546T>C