Allele Registry

Canonical Allele Identifier: PA2827585582

Gene: TCIRG1 HGNC NCBI

ClinVar Variation Id: 991174

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337988.1:p.Phe231Leu	CA6147196 NM_001351059.2:c.693C>A CA381585010 NM_001351059.2:c.691T>C CA381585027 NM_001351059.2:c.693C>G