Canonical Allele Identifier: PA2829982573
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65215
ClinVar RCV Id: RCV000055434 RCV000989440
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Ser1610Pro
CA021390
NM_021055.3:c.4828T>C