Canonical Allele Identifier: PA2827959492
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 655278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Glu1683Gly
CA16032310
NM_001354897.2:c.5048A>G