Canonical Allele Identifier: PA2828419368
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_001357334.1:p.Ser1051Trp
CA045126
NM_001370405.1:c.3152C>G