Canonical Allele Identifier: PA915987497
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 41696
ClinVar RCV Id: RCV000034609 RCV000122196 RCV000054850 RCV000130763 RCV000297382 RCV001080484
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Gly984Ser
CA007165
NM_001162427.2:c.2950G>A