Canonical Allele Identifier: PA2825024534
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr2514Ala
CA048361
NM_000038.6:c.7540A>G