Canonical Allele Identifier: PA2827985055
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537528
ClinVar RCV Id: RCV003538494
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asn1081His
CA16028701
NM_001354900.2:c.3241A>C