Canonical Allele Identifier: PA2827003656
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49529
ClinVar RCV Id: RCV000042789 RCV000254034 RCV001069687
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Trp1128Gly
CA019409
NM_001318827.2:c.3382T>G