Canonical Allele Identifier: PA2827015481
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535914

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Asn1244Ser
CA276753586
NM_001318831.2:c.3731A>G