Canonical Allele Identifier: PA2829040164
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2081928
ClinVar RCV Id: RCV002995724

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372661.1:p.Ala384Ser
CA395406697
NM_001385732.1:c.1150G>T