Canonical Allele Identifier: PA2827009723
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 950491
ClinVar RCV Id: RCV001222211 RCV003163715 RCV004010744
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Pro1402Leu
CA394303002
NM_001318829.2:c.4205C>T