Canonical Allele Identifier: PA2827001167
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467858
ClinVar RCV Id: RCV000540723 RCV002384163 RCV003992321
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Tyr392Cys
CA029149
NM_001318827.2:c.1175A>G