Canonical Allele Identifier: PA2829980097
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486629
ClinVar RCV Id: RCV000573012 RCV000644391 RCV001722536 RCV003230549 RCV003153748 RCV004001153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Val1277Ile
CA049761
NM_021055.3:c.3829G>A