Canonical Allele Identifier: PA2827944890
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1745286

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Asp1698Val
CA16032466
NM_001354895.2:c.5093A>T