Canonical Allele Identifier: PA2828413338
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406114
ClinVar RCV Id: RCV000465409 RCV002451089
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Gly1079Glu
CA16614770
NM_001370404.1:c.3236G>A