Canonical Allele Identifier: PA2826139124
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1047131
ClinVar RCV Id: RCV001351799

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171569.1:p.Ala369Thr
CA395405539
NM_001178098.2:c.1105G>A