Canonical Allele Identifier: PA2827970882
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Lys2332Glu
CA16036732
NM_001354898.2:c.6994A>G