Canonical Allele Identifier: PA2827001005
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50164
ClinVar RCV Id: RCV000043432 RCV000572792 RCV000842561 RCV001084867
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Pro341Leu
CA013884
NM_001318827.2:c.1022C>T