Canonical Allele Identifier: PA2826474221
Gene: BLNK HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245371.1:p.Asp281Gly
CA377715094
NM_001258442.2:c.842A>G