Canonical Allele Identifier: PA2828421839
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 574864
ClinVar RCV Id: RCV000696912 RCV002343495 RCV002477587
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Ala1735Ser
CA394315696
NM_001370405.1:c.5203G>T