Canonical Allele Identifier: PA2825576061
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_001107854.1:p.Gly1302Asp
CA049827
NM_001114382.3:c.3905G>A