Canonical Allele Identifier: PA2825576972
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50095
ClinVar RCV Id: RCV000043361 RCV000820413
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Leu1555Pro
CA020960
NM_001114382.3:c.4664T>C