Canonical Allele Identifier: PA2827111284
Gene: RPS19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1782649
ClinVar RCV Id: RCV002410682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308413.1:p.Leu64Pro
CA406029911
NM_001321484.1:c.191T>C