Canonical Allele Identifier: PA2826474089
Gene: BLNK HGNC NCBI
ClinVar RCV:
RCV003048701
ClinVar Variation:
2135600
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245370.1:p.Asn366Tyr
CA377715064
NM_001258441.2:c.1096A>T