Canonical Allele Identifier: PA2827010011
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 838362
ClinVar RCV Id: RCV001039897 RCV003393797
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Met1500Arg
CA394308151
NM_001318829.2:c.4499T>G