Canonical Allele Identifier: PA2827008484
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 233995
ClinVar RCV Id: RCV000221766 RCV001341323 RCV002251447
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Ser1002Trp
CA045126
NM_001318829.2:c.3005C>G