Canonical Allele Identifier: PA106936
Gene: TCIRG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 5463
ClinVar Variation Id: 552227

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006010.2:p.Gly405Arg
CA117545
NM_006019.4:c.1213G>A
CA381582212
NM_006019.4:c.1213G>C