Canonical Allele Identifier: PA915987460
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 466118
ClinVar RCV Id: RCV000532264 RCV001018500 RCV001821552
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Arg976Trp
CA035767
NM_001162427.2:c.2926C>T