Canonical Allele Identifier: PA891852430
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 572351
ClinVar RCV Id: RCV000693713
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Arg29Lys
CA394301347
NM_000548.5:c.86G>A