Canonical Allele Identifier: PA915986665
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411244
ClinVar RCV Id: RCV000474214
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155898.1:p.Lys121Met
CA16612651
NM_001162426.2:c.362A>T