Canonical Allele Identifier: PA2827585539
Gene: TCIRG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2151108
ClinVar RCV Id: RCV003067908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337988.1:p.Phe193Ser
CA381584440
NM_001351059.2:c.578T>C