Canonical Allele Identifier: PA2828028451
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1758892
ClinVar RCV Id: RCV002385033

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Gln2377Glu
CA16037504
NM_001354903.2:c.7129C>G