Canonical Allele Identifier: PA2828019638
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469920
ClinVar RCV Id: RCV003742679 RCV003338658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asn841Ser
CA16028720
NM_001354906.2:c.2522A>G