Canonical Allele Identifier: PA2825299286
Gene: RPS19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2118121
ClinVar RCV Id: RCV003030319
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001013.1:p.Pro89Arg
CA406030372
NM_001022.3:c.266C>G