Canonical Allele Identifier: PA916040586
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236616
ClinVar RCV Id: RCV000572688 RCV000485173 RCV003153519 RCV002465578 RCV003535624 RCV003998674
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ala1773Val
CA041104
NM_001354896.2:c.5318C>T