Canonical Allele Identifier: PA2829971670
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 187388
ClinVar RCV Id: RCV000167112 RCV000233190 RCV001721086 RCV003995559
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Ala210Val
CA022710
NM_021055.3:c.629C>T