Canonical Allele Identifier: PA293981
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140904
ClinVar RCV Id: RCV000129152 RCV000211901 RCV002514712 RCV003743583 RCV001778746 RCV003997485
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ile632Thr
CA006270
NM_001127510.3:c.1895T>C