Canonical Allele Identifier: PA2825571922
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535900
ClinVar RCV Id: RCV000644123 RCV002386073 RCV004003998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Gly33Asp
CA394301452
NM_001114382.3:c.98G>A