Canonical Allele Identifier: PA2828060398
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1037077
ClinVar RCV Id: RCV001340174
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349106.1:p.Lys587Gln
CA375361005
NM_001362177.1:c.1759A>C