Canonical Allele Identifier: PA645402240
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr2514Ala
CA048361
NM_001127510.3:c.7540A>G