Canonical Allele Identifier: PA2827020907
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468145

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Asn1675Lys
CA394314174
NM_001318832.2:c.5025C>A
CA394314180
NM_001318832.2:c.5025C>G