Canonical Allele Identifier: PA2827975626
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 934037
ClinVar RCV Id: RCV003650659

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Gly991Arg
CA16028023
NM_001354899.2:c.2971G>A
CA16028024
NM_001354899.2:c.2971G>C