Canonical Allele Identifier: PA2828018292
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428176

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Leu639Phe
CA033363
NM_001354906.2:c.1915C>T