Canonical Allele Identifier: PA916040575
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Arg1760Leu
CA16032754
NM_001354896.2:c.5279G>T