Canonical Allele Identifier: PA2573168329
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1692395
ClinVar RCV Id: RCV002258532

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Phe707Ser
CA375361009
NM_000368.5:c.2120T>C