Canonical Allele Identifier: PA2829978697
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468005
ClinVar RCV Id: RCV000527776 RCV000569864 RCV001584294 RCV004527647
ClinVar Variation Id: 578164
ClinVar RCV Id: RCV000701092 RCV001020078 RCV002509519
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Val1077Leu
CA276746154
NM_021055.3:c.3229G>T
CA394286664
NM_021055.3:c.3229G>C