Canonical Allele Identifier: PA2828042690
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Arg1616Leu
CA16032754
NM_001354904.2:c.4847G>T