Canonical Allele Identifier: PA916039630
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469719
ClinVar RCV Id: RCV000554226 RCV000561260 RCV001356454 RCV000764562 RCV002231842 RCV003153714 RCV003493637 RCV003403312 RCV003999361
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Val606Ile
CA029508
NM_001354896.2:c.1816G>A