Canonical Allele Identifier: PA658801428
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 534416

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Met224Leu
CA200900992
NM_000368.5:c.670A>T
CA375371515
NM_000368.5:c.670A>C