Canonical Allele Identifier: PA916023618
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 819976
ClinVar RCV Id: RCV001012958
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Thr595Arg
CA394272807
NM_001318832.2:c.1784C>G