Canonical Allele Identifier: PA2827980421
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2440Pro
CA013665
NM_001354899.2:c.7318T>C