Canonical Allele Identifier: PA2827980714
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470103

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2528Leu
CA048890
NM_001354899.2:c.7583C>T