Canonical Allele Identifier: PA2828420051
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 41736
ClinVar RCV Id: RCV000034653 RCV000054864 RCV000122229 RCV000129666 RCV000231518
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Ala1254Thr
CA019668
NM_001370405.1:c.3760G>A