Canonical Allele Identifier: PA2825576569
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405951
ClinVar RCV Id: RCV000574358 RCV000842193 RCV001085474 RCV004000676
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Gly1449Ser
CA051085
NM_001114382.3:c.4345G>A