Canonical Allele Identifier: PA2829983968
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1507258
ClinVar RCV Id: RCV002009401 RCV003303632
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Gln1736His
CA055156
NM_021055.3:c.5208G>C
CA394315644
NM_021055.3:c.5208G>T