Canonical Allele Identifier: PA2827996251
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1900687
ClinVar RCV Id: RCV003776566
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Pro1701Ser
CA16032868
NM_001354901.2:c.5101C>T