Allele Registry

Canonical Allele Identifier: PA2573201981

Gene: RPL19 HGNC NCBI

ClinVar RCV:

RCV001890048

ClinVar Variation:

1378002

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317129.1:p.Ala9Ser	CA290376093 NM_001330200.1:c.25G>T