Canonical Allele Identifier: PA262622
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49371
ClinVar RCV Id: RCV000042631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Arg1795Leu
CA022452
NM_000548.5:c.5384G>T