Canonical Allele Identifier: PA2827989533
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1758892
ClinVar RCV Id: RCV002385033

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Gln2437Glu
CA16037504
NM_001354900.2:c.7309C>G