Canonical Allele Identifier: PA2828409829
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535920
ClinVar RCV Id: RCV000644150 RCV001010984
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Ile44Thr
CA394301782
NM_001370404.1:c.131T>C