Canonical Allele Identifier: PA916023682
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 385710
ClinVar RCV Id: RCV000424565 RCV001865357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ala634Val
CA16608037
NM_001318832.2:c.1901C>T