Canonical Allele Identifier: PA2827008449
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65283
ClinVar RCV Id: RCV000055504 RCV000498705 RCV002298458
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Leu974Pro
CA018667
NM_001318829.2:c.2921T>C