Canonical Allele Identifier: PA2827111078
Gene: RPS19 HGNC NCBI

Linked Data

ClinVar Variation Id: 640546
ClinVar RCV Id: RCV000793592
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308412.1:p.Ser59Leu
CA915951693
NM_001321483.1:c.175_176delinsCT