Canonical Allele Identifier: PA916023662
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486600
ClinVar RCV Id: RCV000570537 RCV001369719 RCV003459405
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ile621Val
CA394273002
NM_001318832.2:c.1861A>G