Canonical Allele Identifier: PA2825575501
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_001107854.1:p.Gly1123Glu
CA16614770
NM_001114382.3:c.3368G>A