Canonical Allele Identifier: PA2580358986
Gene: BLNK HGNC NCBI

Linked Data

ClinVar Variation Id: 2135600
ClinVar RCV Id: RCV003048701
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_037446.1:p.Asn441Tyr
CA377715064
NM_013314.4:c.1321A>T