Canonical Allele Identifier: PA2828095308
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1477932
ClinVar RCV Id: RCV001973951 RCV002335004 RCV004011038
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Ser1662Arg
CA394314102
NM_001363528.2:c.4984A>C
CA394314115
NM_001363528.2:c.4986C>G
CA394314116
NM_001363528.2:c.4986C>A