Canonical Allele Identifier: PA1139733001
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 923028
ClinVar RCV Id: RCV001183414
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Gly998Ala
CA16028162
NM_001354900.2:c.2993G>C