Canonical Allele Identifier: PA2825577142
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_001107854.1:p.Val1607Met
CA10648023
NM_001114382.3:c.4819G>A