Canonical Allele Identifier: PA2827011004
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468141
ClinVar RCV Id: RCV000543917 RCV002350297 RCV003999325
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Val1596Leu
CA394312457
NM_001318829.2:c.4786G>C
CA394312460
NM_001318829.2:c.4786G>T