Canonical Allele Identifier: PA2828044508
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1018219
ClinVar RCV Id: RCV002543727

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asn1855Lys
CA16034338
NM_001354904.2:c.5565T>A
CA16034339
NM_001354904.2:c.5565T>G