Canonical Allele Identifier: PA2827020154
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 536044

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Arg1473Trp
CA276754888
NM_001318832.2:c.4417C>T