Canonical Allele Identifier: PA2828048464
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 918607
ClinVar RCV Id: RCV001176273

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ala2450Pro
CA16038109
NM_001354904.2:c.7348G>C