Canonical Allele Identifier: PA2829982832
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65289
ClinVar RCV Id: RCV000055511 RCV000163808 RCV000189940 RCV000585252 RCV001081308 RCV004537246
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Glu1636Lys
CA021570
NM_021055.3:c.4906G>A