Canonical Allele Identifier: PA891846205
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 569435
ClinVar RCV Id: RCV000690061 RCV004026347 RCV003999539
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Gln325Arg
CA375368643
NM_000368.5:c.974A>G