Canonical Allele Identifier: PA2829975148
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535965

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Pro674Ser
CA035778
NM_021055.3:c.2020C>T