Canonical Allele Identifier: PA2828049023
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1761379
ClinVar RCV Id: RCV002412380

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Lys2527Asn
CA16038614
NM_001354904.2:c.7581A>C
CA16038615
NM_001354904.2:c.7581A>T