Canonical Allele Identifier: PA2827959859
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411404
ClinVar RCV Id: RCV000566066 RCV001836824 RCV003766566 RCV004001938
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ile1789Met
CA041612
NM_001354897.2:c.5367A>G