Canonical Allele Identifier: PA2825629684
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1799325
ClinVar RCV Id: RCV002444172
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Glu1020Val
CA16028034
NM_001127510.3:c.3059A>T