Canonical Allele Identifier: PA2825572568
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406031
ClinVar RCV Id: RCV000458732 RCV002365618
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Pro232Ser
CA056156
NM_001114382.3:c.694C>T