Canonical Allele Identifier: PA167921
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142268
ClinVar RCV Id: RCV000131289 RCV002228321
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Val1463Ile
CA009548
NM_001127511.3:c.4387G>A