Canonical Allele Identifier: PA348956
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 220442
ClinVar RCV Id: RCV002515525 RCV003650466 RCV000775337 RCV003997638
ClinVar Variation Id: 470028
ClinVar RCV Id: RCV001189643 RCV003742749
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asp1976Glu
CA043621
NM_001127511.3:c.5928C>G
CA16034426
NM_001127511.3:c.5928C>A