Canonical Allele Identifier: PA2827111085
Gene: RPS19 HGNC NCBI

Linked Data

ClinVar Variation Id: 463372
ClinVar RCV Id: RCV000538681 RCV001702674 RCV003900162
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308412.1:p.Arg62Gln
CA406029872
NM_001321483.1:c.185G>A