Canonical Allele Identifier: PA2828412773
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2092647
ClinVar RCV Id: RCV003008263
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Lys906Glu
CA394279500
NM_001370404.1:c.2716A>G