Canonical Allele Identifier: PA2825644668
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760781
ClinVar RCV Id: RCV002410000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Lys2591Glu
CA16038330
NM_001127511.3:c.7771A>G