Canonical Allele Identifier: PA2825439714
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535864
ClinVar RCV Id: RCV000644075

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Pro1714Ala
CA394315679
NM_001077183.3:c.5140C>G