Canonical Allele Identifier: PA2827009101
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 448730
ClinVar RCV Id: RCV000516748 RCV001857933
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Gly1210Asp
CA049827
NM_001318829.2:c.3629G>A