Canonical Allele Identifier: PA2827010797
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49518
ClinVar RCV Id: RCV000042778 RCV001852890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Tyr1456Cys
CA020940
NM_001318829.2:c.4367A>G