Canonical Allele Identifier: PA2828060408
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2620304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349106.1:p.Ala592Gly
CA375360931
NM_001362177.1:c.1775C>G