Canonical Allele Identifier: PA916023680
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64889
ClinVar RCV Id: RCV000055090 RCV000574001 RCV000644057 RCV004537239 RCV001562207
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Arg633Trp
CA016088
NM_001318832.2:c.1897C>T