Canonical Allele Identifier: PA2825024468
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser2497Thr
CA16037620
NM_000038.6:c.7489T>A