Canonical Allele Identifier: PA2825439913
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_001070651.1:p.Val1606Phe
CA021508
NM_001077183.3:c.4816G>T