Canonical Allele Identifier: PA645390336
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 318804

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001761.3:p.Pro176Leu
CA7988382
NM_001770.6:c.527C>T