Canonical Allele Identifier: PA2828055328
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2774891
ClinVar RCV Id: RCV003586071

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Pro864Ala
CA16028057
NM_001354905.2:c.2590C>G