Canonical Allele Identifier: PA913200440
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 628704
ClinVar RCV Id: RCV000773365
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser2552Gly
CA16037959
NM_001127510.3:c.7654A>G