Canonical Allele Identifier: PA2828409792
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486639
ClinVar RCV Id: RCV000563255 RCV000644191
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Gly33Ser
CA056868
NM_001370404.1:c.97G>A