Canonical Allele Identifier: PA106927
Gene: TCIRG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 975009
ClinVar RCV Id: RCV001251405 RCV001375862 RCV001814292 RCV002570450
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006010.2:p.Asp517Asn
CA6147157
NM_006019.4:c.1549G>A