Canonical Allele Identifier: PA645486442
Gene: TCIRG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 305821

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006010.2:p.Ala778Val
CA6147502
NM_006019.4:c.2333C>T