Canonical Allele Identifier: PA916039624
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428153
ClinVar Variation Id: 1779244
ClinVar RCV Id: RCV002401443

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Lys599Asn
CA16025124
NM_001354896.2:c.1797G>C
CA16025125
NM_001354896.2:c.1797G>T