Canonical Allele Identifier: PA2828414659
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535877
ClinVar RCV Id: RCV000644095 RCV002331186 RCV004003991
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Ser1463Tyr
CA051496
NM_001370404.1:c.4388C>A