Canonical Allele Identifier: PA2828092645
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1016670
ClinVar RCV Id: RCV001315705
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Arg901Leu
CA394279443
NM_001363528.2:c.2702G>T