Canonical Allele Identifier: PA2827959584
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485156

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ala1710Thr
CA16032477
NM_001354897.2:c.5128G>A