Canonical Allele Identifier: PA2829040126
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2054666
ClinVar RCV Id: RCV002932883
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372661.1:p.Thr285Ser
CA395405594
NM_001385732.1:c.853A>T
CA395405603
NM_001385732.1:c.854C>G