Canonical Allele Identifier: PA2825024598
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 957710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser2535Gly
CA16037848
NM_000038.6:c.7603A>G