Canonical Allele Identifier: PA2827977986
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1717624
ClinVar RCV Id: RCV003743868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ala1697Ser
CA16032639
NM_001354899.2:c.5089G>T