Canonical Allele Identifier: PA2827990117
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537551

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Lys2612Glu
CA16038609
NM_001354900.2:c.7834A>G