Canonical Allele Identifier: PA916023004
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405953
ClinVar RCV Id: RCV000575419 RCV000468858 RCV001567190
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Pro854Leu
CA045588
NM_001318831.2:c.2561C>T