Canonical Allele Identifier: PA2827014733
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535915

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Asn1026Ser
CA394293642
NM_001318831.2:c.3077A>G