Canonical Allele Identifier: PA2827945046
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Arg1742Leu
CA16032754
NM_001354895.2:c.5225G>T