Canonical Allele Identifier: PA2827004692
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 848503
ClinVar RCV Id: RCV001052273 RCV002339262 RCV003156307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Glu1425Gln
CA394304419
NM_001318827.2:c.4273G>C