Canonical Allele Identifier: PA2827959405
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_001341826.1:p.Val1651Leu
CA16032109
NM_001354897.2:c.4951G>C
CA16032110
NM_001354897.2:c.4951G>T