Canonical Allele Identifier: PA262948
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49830
ClinVar RCV Id: RCV000043096 RCV001050539 RCV001022358
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Ser1454Gly
CA020332
NM_000548.5:c.4360A>G