Canonical Allele Identifier: PA2828412614
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237996
ClinVar RCV Id: RCV000230556 RCV001091442 RCV002429101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Tyr857Cys
CA10583311
NM_001370404.1:c.2570A>G