Canonical Allele Identifier: PA2829981326
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207685
ClinVar RCV Id: RCV000189932 RCV000218843 RCV000458406 RCV003996870
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Glu1433Lys
CA051101
NM_021055.3:c.4297G>A