Canonical Allele Identifier: PA2573221914
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1448752

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001761.3:p.Ala387Glu
CA7988582
NM_001770.6:c.1160C>A