Canonical Allele Identifier: PA2829981338
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1052237
ClinVar RCV Id: RCV001360380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Asp1435Ala
CA394302259
NM_021055.3:c.4304A>C