Canonical Allele Identifier: PA2829982394
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 318334
ClinVar RCV Id: RCV000371761 RCV001023201 RCV000839227 RCV001079540 RCV004537797
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Val1587Met
CA10648023
NM_021055.3:c.4759G>A