Canonical Allele Identifier: PA2828022841
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482483
ClinVar Variation Id: 1744135
ClinVar RCV Id: RCV002351274

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Val1358Leu
CA16032109
NM_001354906.2:c.4072G>C
CA16032110
NM_001354906.2:c.4072G>T