Canonical Allele Identifier: PA2826139139
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1717462
ClinVar RCV Id: RCV002296371
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171569.1:p.Glu404Lys
CA395406014
NM_001178098.2:c.1210G>A