Canonical Allele Identifier: PA2828094270
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468085
ClinVar RCV Id: RCV000533905 RCV001022339 RCV003999315
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Arg1385Gly
CA050943
NM_001363528.2:c.4153C>G