Canonical Allele Identifier: PA2827978717
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 350415
ClinVar RCV Id: RCV000362266 RCV000775335 RCV003317196 RCV001821073 RCV002520290
ClinVar Variation Id: 3230807
ClinVar RCV Id: RCV004522921
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Thr1919Ser
CA043197
NM_001354899.2:c.5756C>G
CA16034103
NM_001354899.2:c.5755A>T