Canonical Allele Identifier: PA2827011657
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 41750
ClinVar RCV Id: RCV000034667 RCV002257374 RCV001084556 RCV003996175
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Arg108Gly
CA023120
NM_001318831.2:c.322C>G