Canonical Allele Identifier: PA2825021390
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1719410
ClinVar RCV Id: RCV003743893
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Val1708Ala
CA16032528
NM_000038.6:c.5123T>C