Canonical Allele Identifier: PA2829040128
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2613521
ClinVar RCV Id: RCV003362399

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372661.1:p.Ser294Arg
CA395405713
NM_001385732.1:c.880A>C
CA395405726
NM_001385732.1:c.882C>A
CA395405727
NM_001385732.1:c.882C>G