Canonical Allele Identifier: PA2829040130
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1448752

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372661.1:p.Ala298Glu
CA7988582
NM_001385732.1:c.893C>A