Allele Registry

Canonical Allele Identifier: PA891866112

Gene: RPS19 HGNC NCBI

ClinVar RCV:

RCV000462953

ClinVar Variation:

412282

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308414.1:p.Thr132Ile	CA16616275 NM_001321485.1:c.395C>T