Canonical Allele Identifier: PA645400389
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231079
ClinVar RCV Id: RCV000216852 RCV000589084 RCV002229236
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Val1822Gly
CA10578404
NM_001127510.3:c.5465T>G