Canonical Allele Identifier: PA2826139167
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1920790
ClinVar RCV Id: RCV002591302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171569.1:p.Val472Phe
CA395406681
NM_001178098.2:c.1414G>T