Canonical Allele Identifier: PA2828013467
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1317229
ClinVar RCV Id: RCV001759101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ile2523Ser
CA16038805
NM_001354905.2:c.7568T>G