Canonical Allele Identifier: PA2825644437
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759762
ClinVar RCV Id: RCV002396180
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Glu2516Gln
CA16037840
NM_001127511.3:c.7546G>C