Canonical Allele Identifier: PA2828413168
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406055
ClinVar RCV Id: RCV000457622 RCV002446790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Arg1034Gln
CA044900
NM_001370404.1:c.3101G>A