Canonical Allele Identifier: PA2827998682
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1511850
ClinVar RCV Id: RCV003773417
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ala2442Ser
CA16037645
NM_001354901.2:c.7324G>T