Canonical Allele Identifier: PA916023178
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486639
ClinVar RCV Id: RCV000563255 RCV000644191
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Gly44Ser
CA056868
NM_001318832.2:c.130G>A