Canonical Allele Identifier: PA2825024861
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1719845
ClinVar RCV Id: RCV003743897

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Lys2602Arg
CA16038286
NM_000038.6:c.7805A>G