Canonical Allele Identifier: PA2826474221
Gene: BLNK HGNC NCBI

Linked Data

ClinVar Variation Id: 1478872
ClinVar RCV Id: RCV001990804
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Amino-acid Alleles

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