Canonical Allele Identifier: PA2828414380
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468077
ClinVar RCV Id: RCV000547245 RCV002330900 RCV003999311
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Ser1387Leu
CA050780
NM_001370404.1:c.4160C>T