Canonical Allele Identifier: PA2827966763
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2705140
ClinVar RCV Id: RCV003536367
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Thr1087Ser
CA16028644
NM_001354898.2:c.3259A>T