Canonical Allele Identifier: PA2828007932
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490304
ClinVar RCV Id: RCV000581741 RCV003653207
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Val1616Ile
CA041569
NM_001354905.2:c.4846G>A