Canonical Allele Identifier: PA2828048322
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1009233
ClinVar RCV Id: RCV003770591

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Leu2432Phe
CA16037997
NM_001354904.2:c.7294C>T