Canonical Allele Identifier: PA2827009519
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 497137
ClinVar RCV Id: RCV000592461 RCV001084298 RCV002331007
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Pro1343Thr
CA394301760
NM_001318829.2:c.4027C>A