Canonical Allele Identifier: PA2828413646
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535985
ClinVar RCV Id: RCV000644234
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Glu1169Val
CA394291819
NM_001370404.1:c.3506A>T