Canonical Allele Identifier: PA2827001085
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237961
ClinVar RCV Id: RCV000226213 RCV000568157
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Glu368Gln
CA028805
NM_001318827.2:c.1102G>C