Canonical Allele Identifier: PA2827018605
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467994
ClinVar RCV Id: RCV000525625 RCV004024048
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Val1034Leu
CA044723
NM_001318832.2:c.3100G>C