Canonical Allele Identifier: PA2829983225
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49931
ClinVar RCV Id: RCV000043198 RCV000201077
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Arg1670Pro
CA021846
NM_021055.3:c.5009G>C