Canonical Allele Identifier: PA2827315261
Gene: BLK HGNC NCBI

Linked Data

ClinVar Variation Id: 2428692
ClinVar RCV Id: RCV003120293
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317394.1:p.Tyr394His
CA370316768
NM_001330465.2:c.1180T>C