Canonical Allele Identifier: PA2827017986
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2564616
ClinVar RCV Id: RCV003297048

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Pro680Ser
CA394274452
NM_001318832.2:c.2038C>T