Canonical Allele Identifier: PA2827008971
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468039
ClinVar RCV Id: RCV000526703 RCV002350296
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Lys1170Arg
CA048406
NM_001318829.2:c.3509A>G