Canonical Allele Identifier: PA2827015669
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1400703
ClinVar RCV Id: RCV001911450
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Gln1292Arg
CA394304672
NM_001318831.2:c.3875A>G