Canonical Allele Identifier: PA2828410498
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 536104
ClinVar RCV Id: RCV001026437 RCV000644409 RCV003328614
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Asn248Ser
CA056283
NM_001370404.1:c.743A>G