Canonical Allele Identifier: PA2828018476
Gene: APC HGNC NCBI
ClinVar Allele:
520484
ClinVar RCV:
RCV003538428
ClinVar Variation:
537427
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser665Pro
CA16027530
NM_001354906.2:c.1993T>C