Canonical Allele Identifier: PA2828012220
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1758948
ClinVar RCV Id: RCV002385089
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Val2323Ala
CA16037539
NM_001354905.2:c.6968T>C