Canonical Allele Identifier: PA2828410651
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49402
ClinVar RCV Id: RCV000042662 RCV002513623 RCV003333730
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Gly294Arg
CA023075
NM_001370404.1:c.880G>A
CA394315117
NM_001370404.1:c.880G>C