Canonical Allele Identifier: PA645398926
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_001120982.1:p.Lys581Asn
CA16025124
NM_001127510.3:c.1743G>C
CA16025125
NM_001127510.3:c.1743G>T