Canonical Allele Identifier: PA2825644854
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 851804
ClinVar RCV Id: RCV002240266
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asn2649Ser
CA16038710
NM_001127511.3:c.7946A>G