Canonical Allele Identifier: PA658805102
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535873
ClinVar RCV Id: RCV000644091 RCV000984876
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Pro1675Gln
CA394311256
NM_000548.5:c.5024C>A