Canonical Allele Identifier: PA2825634952
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1022071

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Lys2412Glu
CA16037088
NM_001127510.3:c.7234A>G