Canonical Allele Identifier: PA2827019137
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1733615
ClinVar RCV Id: RCV002452497

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Pro1185His
CA394291998
NM_001318832.2:c.3554C>A