Canonical Allele Identifier: PA2828012759
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 243109

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Val2595Ala
CA049793
NM_001354902.2:c.7784T>C