Canonical Allele Identifier: PA2826473923
Gene: BLNK HGNC NCBI

Linked Data

ClinVar Variation Id: 2135600
ClinVar RCV Id: RCV003048701

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245369.1:p.Asn389Tyr
CA377715064
NM_001258440.2:c.1165A>T