Canonical Allele Identifier: PA1139704371
Gene: BLK HGNC NCBI

Linked Data

ClinVar Variation Id: 912039
ClinVar RCV Id: RCV001164968
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001706.2:p.Glu471Gln
CA370316823
NM_001715.3:c.1411G>C