Canonical Allele Identifier: PA2829971237
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65379
ClinVar RCV Id: RCV000055607 RCV000575914 RCV000465969 RCV001557660 RCV003996482
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.His152Asp
CA020642
NM_021055.3:c.454C>G