Canonical Allele Identifier: PA2828420584
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_001357334.1:p.Arg1408Gly
CA050943
NM_001370405.1:c.4222C>G