Canonical Allele Identifier: PA2825919608
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 207622

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155898.1:p.Asn1156Asp
CA319266
NM_001162426.2:c.3466A>G