Canonical Allele Identifier: PA2827975986
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 823680
ClinVar RCV Id: RCV001020123 RCV003769524
ClinVar Variation Id: 2720472
ClinVar RCV Id: RCV003537888
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Val1097Leu
CA16028725
NM_001354899.2:c.3289G>C
CA16028726
NM_001354899.2:c.3289G>T