Canonical Allele Identifier: PA262476
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49177
ClinVar RCV Id: RCV000042433 RCV001388105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Arg611Gly
CA015905
NM_000548.5:c.1831C>G