Canonical Allele Identifier: PA2741886637
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2537218
ClinVar RCV Id: RCV003271497

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001761.3:p.Asn423Tyr
CA395406192
NM_001770.6:c.1267A>T