Canonical Allele Identifier: PA2827971887
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3005182
ClinVar RCV Id: RCV003868309
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ile2636Val
CA16038663
NM_001354898.2:c.7906A>G