Canonical Allele Identifier: PA2828410690
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_001357333.1:p.Arg308Gly
CA023120
NM_001370404.1:c.922C>G