Canonical Allele Identifier: PA2828416000
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 161398
ClinVar RCV Id: RCV000148918 RCV000226143 RCV000571093 RCV001704075 RCV004544347 RCV003153433
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Asn56Ser
CA015434
NM_001370405.1:c.167A>G