Canonical Allele Identifier: PA2827964209
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2452729
ClinVar RCV Id: RCV003177503
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser269Cys
CA16023246
NM_001354898.2:c.806C>G