Canonical Allele Identifier: PA2825633478
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 924017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser1706Pro
CA16032513
NM_001127510.3:c.5116T>C