Canonical Allele Identifier: PA2828009522
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_001341831.1:p.Val1617Ala
CA16032528
NM_001354902.2:c.4850T>C