Canonical Allele Identifier: PA2827015027
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207752
ClinVar RCV Id: RCV000190029 RCV000644243 RCV001021792 RCV003996895
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Gly1112Asp
CA050325
NM_001318831.2:c.3335G>A