Canonical Allele Identifier: PA2828411724
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49643
ClinVar RCV Id: RCV000042905 RCV000189989 RCV000539587 RCV000768117 RCV000491813
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Arg611Trp
CA015914
NM_001370404.1:c.1831C>T
CA645594269
NM_001370404.1:c.1830_1831delinsTT