Canonical Allele Identifier: PA2827008874
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1050887
ClinVar RCV Id: RCV001358846
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Leu1136Met
CA394292351
NM_001318829.2:c.3406C>A