Canonical Allele Identifier: PA2827998858
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470103

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2497Leu
CA048890
NM_001354901.2:c.7490C>T