Canonical Allele Identifier: PA2827980842
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1692385
ClinVar RCV Id: RCV002257179
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2566Ala
CA16038234
NM_001354899.2:c.7696T>G