Canonical Allele Identifier: PA2826139129
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2054666
ClinVar RCV Id: RCV002932883
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171569.1:p.Thr374Ser
CA395405594
NM_001178098.2:c.1120A>T
CA395405603
NM_001178098.2:c.1121C>G