Canonical Allele Identifier: PA2828421464
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49441
ClinVar RCV Id: RCV000042701 RCV000822377 RCV002336160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Lys1646Glu
CA021601
NM_001370405.1:c.4936A>G