Canonical Allele Identifier: PA2825439800
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_001070651.1:p.Glu1734Asp
CA16615209
NM_001077183.3:c.5202G>T
CA394316180
NM_001077183.3:c.5202G>C