Canonical Allele Identifier: PA2827315268
Gene: BLK HGNC NCBI

Linked Data

ClinVar Variation Id: 2427877
ClinVar RCV Id: RCV003116848
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317394.1:p.Glu413Asp
CA4630525
NM_001330465.2:c.1239G>C
CA370316959
NM_001330465.2:c.1239G>T