Canonical Allele Identifier: PA2827009629
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238051
ClinVar RCV Id: RCV000227544 RCV000572080 RCV003153526
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Glu1375Gly
CA051259
NM_001318829.2:c.4124A>G