Canonical Allele Identifier: PA916023103
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468020
ClinVar RCV Id: RCV000534200 RCV001574195 RCV002258956
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Pro932Ser
CA394289363
NM_001318831.2:c.2794C>T