Canonical Allele Identifier: PA2827315059
Gene: BLK HGNC NCBI

Linked Data

ClinVar Variation Id: 619207
ClinVar RCV Id: RCV000758188
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317394.1:p.Lys13Asn
CA4629772
NM_001330465.2:c.39G>C
CA370311617
NM_001330465.2:c.39G>T