Canonical Allele Identifier: PA2825571927
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486619
ClinVar RCV Id: RCV000570293 RCV002530345
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Lys34Arg
CA027990
NM_001114382.3:c.101A>G