Canonical Allele Identifier: PA916023990
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12405
ClinVar RCV Id: RCV000013214 RCV000042482 RCV003441714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Arg916Gly
CA017936
NM_001318832.2:c.2746C>G