Canonical Allele Identifier: PA2828029295
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760974

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asn2341Lys
CA16038436
NM_001354906.2:c.7023T>A
CA16038437
NM_001354906.2:c.7023T>G