Canonical Allele Identifier: PA2828421391
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_001357334.1:p.Ile1629Val
CA053492
NM_001370405.1:c.4885A>G