Canonical Allele Identifier: PA2825569072
Gene: BLNK HGNC NCBI

Linked Data

ClinVar Variation Id: 1059928
ClinVar RCV Id: RCV001369290
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107566.1:p.Asp343Glu
CA5623174
NM_001114094.2:c.1029T>G
CA377716838
NM_001114094.2:c.1029T>A