Canonical Allele Identifier: PA2825633466
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 964536

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ala1700Pro
CA16032478
NM_001127510.3:c.5098G>C