Canonical Allele Identifier: PA2829978476
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141472
ClinVar RCV Id: RCV000130015 RCV000189914 RCV000471098 RCV003477541
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Pro1049Leu
CA018797
NM_021055.3:c.3146C>T