Canonical Allele Identifier: PA2828015339
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1316460

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ile163Leu
CA16024229
NM_001354906.2:c.487A>C