Canonical Allele Identifier: PA913196445
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 624103
ClinVar RCV Id: RCV000762218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001761.3:p.Ala390Val
CA395405823
NM_001770.6:c.1169C>T