Canonical Allele Identifier: PA2827020908
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1025177
ClinVar RCV Id: RCV001325462

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Asn1675Ser
CA054360
NM_001318832.2:c.5024A>G