Canonical Allele Identifier: PA2829984006
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1478025
ClinVar RCV Id: RCV001998504 RCV003303552
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Ala1739Thr
CA394315690
NM_021055.3:c.5215G>A