Canonical Allele Identifier: PA2828415252
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406102
ClinVar RCV Id: RCV000466909 RCV001023422 RCV001538711
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Ile1628Val
CA053492
NM_001370404.1:c.4882A>G