Canonical Allele Identifier: PA916039609
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233448
ClinVar RCV Id: RCV000213578 RCV000779711 RCV001572567 RCV003743674 RCV003998557
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Arg582Gln
CA029022
NM_001354896.2:c.1745G>A