Canonical Allele Identifier: PA2829978753
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 536003
ClinVar RCV Id: RCV000644263 RCV001020148 RCV000765272 RCV003222074
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Arg1084Gln
CA046441
NM_021055.3:c.3251G>A