Canonical Allele Identifier: PA2826139150
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1995716
ClinVar RCV Id: RCV002796795
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171569.1:p.Asn426Ser
CA395406221
NM_001178098.2:c.1277A>G