Canonical Allele Identifier: PA2826139172
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1347599
ClinVar RCV Id: RCV002050639

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171569.1:p.His482Pro
CA395406946
NM_001178098.2:c.1445A>C