Canonical Allele Identifier: PA2827016709
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_001305760.1:p.Glu1557Asp
CA16615209
NM_001318831.2:c.4671G>T
CA394316180
NM_001318831.2:c.4671G>C