Allele Registry

Canonical Allele Identifier: PA3057458030

Gene: RPS19 HGNC NCBI

ClinVar Allele:

3709766

ClinVar RCV:

RCV005028655

ClinVar Variation:

3583915

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308414.1:p.Val15Ile	CA9465261 NM_001321485.1:c.43G>A