Canonical Allele Identifier: PA2826139020
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1362698
ClinVar RCV Id: RCV001934546

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171569.1:p.Pro109Ser
CA7988330
NM_001178098.2:c.325C>T