Canonical Allele Identifier: PA2828411764
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64889
ClinVar RCV Id: RCV000055090 RCV000574001 RCV000644057 RCV004537239 RCV001562207
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Arg622Trp
CA016088
NM_001370404.1:c.1864C>T