Canonical Allele Identifier: PA2826138974
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1494140
ClinVar RCV Id: RCV002012807
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171569.1:p.Leu11Phe
CA7988256
NM_001178098.2:c.31C>T