Canonical Allele Identifier: PA2828413638
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49529
ClinVar RCV Id: RCV000042789 RCV000254034 RCV001069687
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Trp1164Gly
CA019409
NM_001370404.1:c.3490T>G