Canonical Allele Identifier: PA2828413561
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 384002
ClinVar RCV Id: RCV000435796 RCV001020594 RCV001797719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Ala1141Val
CA16607153
NM_001370404.1:c.3422C>T