Canonical Allele Identifier: PA215821
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 41750
ClinVar RCV Id: RCV000034667 RCV002257374 RCV001084556 RCV003996175
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Arg308Gly
CA023120
NM_000548.5:c.922C>G