Canonical Allele Identifier: PA191923
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64847
ClinVar RCV Id: RCV000055045 RCV000475134 RCV000164851 RCV001703956
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Val1291Ile
CA019604
NM_000548.5:c.3871G>A