Canonical Allele Identifier: PA2828012699
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470103

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser2396Leu
CA048890
NM_001354905.2:c.7187C>T