Canonical Allele Identifier: PA2827986792
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482483
ClinVar RCV Id: RCV000573603 RCV003476337
ClinVar Variation Id: 1744135
ClinVar RCV Id: RCV002351274
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Val1600Leu
CA16032109
NM_001354900.2:c.4798G>C
CA16032110
NM_001354900.2:c.4798G>T