Canonical Allele Identifier: PA916023908
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49587
ClinVar RCV Id: RCV000042848 RCV001250499
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Leu819Ser
CA017395
NM_001318832.2:c.2456T>C