Canonical Allele Identifier: PA916039538
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482257

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Thr514Ile
CA16024566
NM_001354896.2:c.1541C>T