Canonical Allele Identifier: PA2827010027
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49327
ClinVar RCV Id: RCV000042587 RCV001383217
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.His1505Tyr
CA021147
NM_001318829.2:c.4513C>T