Canonical Allele Identifier: PA2829970313
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 655432
ClinVar RCV Id: RCV000811607
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Thr41Ser
CA394301697
NM_021055.3:c.121A>T
CA394301701
NM_021055.3:c.122C>G