Canonical Allele Identifier: PA2827018668
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406094
ClinVar RCV Id: RCV000463902 RCV000571612
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ser1052Leu
CA16614705
NM_001318832.2:c.3155C>T