Canonical Allele Identifier: PA2828420691
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 641928
ClinVar RCV Id: RCV000795284
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Asp1435Val
CA394302256
NM_001370405.1:c.4304A>T