Canonical Allele Identifier: PA658680268
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468024
ClinVar RCV Id: RCV000528192 RCV004024050
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Leu119Arg
CA394306574
NM_000548.5:c.356T>G