Canonical Allele Identifier: PA916023099
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406059
ClinVar RCV Id: RCV000841759 RCV001082094 RCV001020514
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Arg930Trp
CA047295
NM_001318831.2:c.2788C>T