Canonical Allele Identifier: PA211339
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135716
ClinVar RCV Id: RCV000131625 RCV000148359 RCV000211933 RCV001719892 RCV003905173 RCV003743581 RCV003153405 RCV000987581 RCV001151806
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ile2329Val
CA012738
NM_001127510.3:c.6985A>G