Canonical Allele Identifier: PA2828421644
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406050
ClinVar RCV Id: RCV000473435 RCV001023737 RCV001546269
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Pro1690Leu
CA054450
NM_001370405.1:c.5069C>T