Canonical Allele Identifier: PA2830386228
Gene: IL21R HGNC NCBI

Linked Data

ClinVar Variation Id: 1678067
ClinVar RCV Id: RCV002224658

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_851564.1:p.Phe147Leu
CA395302045
NM_181078.3:c.439T>C
CA395302056
NM_181078.3:c.441C>A
CA395302059
NM_181078.3:c.441C>G