Canonical Allele Identifier: PA916042489
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 630669
ClinVar RCV Id: RCV000776622 RCV001856132
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser966Cys
CA16028731
NM_001354905.2:c.2896A>T