Canonical Allele Identifier: PA2826473897
Gene: BLNK HGNC NCBI

Linked Data

ClinVar Variation Id: 444234

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245369.1:p.Ile308Thr
CA5623258
NM_001258440.2:c.923T>C