Canonical Allele Identifier: PA2828029647
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1761670
ClinVar RCV Id: RCV002419243

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Arg2390Ile
CA16038747
NM_001354906.2:c.7169G>T