Canonical Allele Identifier: PA162586
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 64699
ClinVar RCV Id: RCV000054874 RCV000122199 RCV000465974 RCV000568811 RCV001618239
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Phe285Val
CA008327
NM_000368.5:c.853T>G