Canonical Allele Identifier: PA2827971731
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3071818
ClinVar RCV Id: RCV004016312

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Lys2591Glu
CA16038378
NM_001354898.2:c.7771A>G