Canonical Allele Identifier: PA2826474198
Gene: BLNK HGNC NCBI

Linked Data

ClinVar Variation Id: 444234

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245371.1:p.Ile203Thr
CA5623258
NM_001258442.2:c.608T>C