Canonical Allele Identifier: PA2827002974
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535970
ClinVar RCV Id: RCV000644215 RCV001016700
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Glu905Gly
CA276742132
NM_001318827.2:c.2714A>G