Canonical Allele Identifier: PA2828048292
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760043

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser2429Ala
CA16037981
NM_001354904.2:c.7285T>G