Canonical Allele Identifier: PA2829040166
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1694790
ClinVar RCV Id: RCV002262510
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372661.1:p.Ser391Arg
CA395406907
NM_001385732.1:c.1171A>C
CA395406925
NM_001385732.1:c.1173C>A
CA395406928
NM_001385732.1:c.1173C>G