Canonical Allele Identifier: PA2828048479
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1692381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser2452Pro
CA16038121
NM_001354904.2:c.7354T>C