Canonical Allele Identifier: PA916040613
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_001341825.1:p.Ile1797Met
CA041612
NM_001354896.2:c.5391A>G