Canonical Allele Identifier: PA2828421930
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405970
ClinVar RCV Id: RCV000465811 RCV002348292
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Glu1754Asp
CA16615209
NM_001370405.1:c.5262G>T
CA394316180
NM_001370405.1:c.5262G>C