Canonical Allele Identifier: PA2829040161
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1920790
ClinVar RCV Id: RCV002591302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372661.1:p.Val383Phe
CA395406681
NM_001385732.1:c.1147G>T