Canonical Allele Identifier: PA2826139120
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2111236
ClinVar RCV Id: RCV003022561
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171569.1:p.Arg363Gly
CA395405457
NM_001178098.2:c.1087C>G