Canonical Allele Identifier: PA2827947459
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1758892
ClinVar RCV Id: RCV002385033

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Gln2478Glu
CA16037504
NM_001354895.2:c.7432C>G