Canonical Allele Identifier: PA2829040121
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1047131
ClinVar RCV Id: RCV001351799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372661.1:p.Ala280Thr
CA395405539
NM_001385732.1:c.838G>A