Canonical Allele Identifier: PA2825635148
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759598
ClinVar RCV Id: RCV002394098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.His2526Gln
CA16037798
NM_001127510.3:c.7578T>A
CA16037799
NM_001127510.3:c.7578T>G