Canonical Allele Identifier: PA2827019065
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406069
ClinVar RCV Id: RCV000570432 RCV000461845 RCV001662421 RCV004000712
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ala1162Val
CA047499
NM_001318832.2:c.3485C>T