Canonical Allele Identifier: PA106920
Gene: TCIRG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 5464

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006010.2:p.Arg444Leu
CA117547
NM_006019.4:c.1331G>T