Canonical Allele Identifier: PA916040839
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.His1983Arg
CA16034228
NM_001354896.2:c.5948A>G