Canonical Allele Identifier: PA2827010013
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2497447
ClinVar RCV Id: RCV003213902
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Met1500Val
CA394308148
NM_001318829.2:c.4498A>G