Canonical Allele Identifier: PA2829982769
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65153
ClinVar RCV Id: RCV000055369 RCV002336203 RCV001342211
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Val1630Phe
CA021508
NM_021055.3:c.4888G>T