Canonical Allele Identifier: PA2829980241
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207679
ClinVar RCV Id: RCV000189924 RCV001053943 RCV002372158
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Glu1300Asp
CA050218
NM_021055.3:c.3900G>C
CA394299242
NM_021055.3:c.3900G>T