Canonical Allele Identifier: PA916022901
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406017
ClinVar RCV Id: RCV000466214 RCV000572112 RCV002510893 RCV004000698
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Val25Met
CA056118
NM_001318831.2:c.73G>A