Canonical Allele Identifier: PA2829981392
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535914

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Asn1445Ser
CA276753586
NM_021055.3:c.4334A>G