Canonical Allele Identifier: PA2827013172
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 384076
ClinVar RCV Id: RCV000439541 RCV000470228 RCV001014141 RCV004000404
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Pro477Leu
CA035873
NM_001318831.2:c.1430C>T