Canonical Allele Identifier: PA916039569
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490215
ClinVar RCV Id: RCV000582026 RCV002298697 RCV003492109 RCV003537246
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Arg545Thr
CA16024760
NM_001354896.2:c.1634G>C