Canonical Allele Identifier: PA2828409992
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406038
ClinVar RCV Id: RCV000471856 RCV001797088 RCV002436401 RCV004533162 RCV004000706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Pro94Leu
CA042049
NM_001370404.1:c.281C>T