Canonical Allele Identifier: PA2828419892
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 318328
ClinVar RCV Id: RCV000356278 RCV000470026 RCV001020999
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Arg1202Trp
CA048198
NM_001370405.1:c.3604C>T