Canonical Allele Identifier: PA170627
Gene: TCIRG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 127173
ClinVar RCV Id: RCV000224333 RCV000133575 RCV000663355
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006010.2:p.Arg736Ser
CA170625
NM_006019.4:c.2206C>A