Canonical Allele Identifier: PA2829983485
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238077
ClinVar RCV Id: RCV000234330 RCV002338712 RCV003469153 RCV003223629
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Asp1691Val
CA10583344
NM_021055.3:c.5072A>T