Canonical Allele Identifier: PA319536
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207755
ClinVar RCV Id: RCV000475369 RCV000574084
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Ser1526Tyr
CA319534
NM_000548.5:c.4577C>A