Canonical Allele Identifier: PA2825572021
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406100
ClinVar RCV Id: RCV000459248 RCV002411435
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Cys65Arg
CA16614896
NM_001114382.3:c.193T>C