Canonical Allele Identifier: PA2829971302
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535868
ClinVar RCV Id: RCV000644082 RCV001023148 RCV004003989
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Asp162Asn
CA394309028
NM_021055.3:c.484G>A