Canonical Allele Identifier: PA2827959833
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411356

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Lys1780Glu
CA041323
NM_001354897.2:c.5338A>G