Canonical Allele Identifier: PA2580257508
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2054666
ClinVar RCV Id: RCV002932883

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001761.3:p.Thr374Ser
CA395405594
NM_001770.6:c.1120A>T
CA395405603
NM_001770.6:c.1121C>G