Allele Registry

Canonical Allele Identifier: PA2825230486

Gene: RPL19 HGNC NCBI

ClinVar RCV:

RCV001890048

ClinVar Variation:

1378002

HGVS (amino-acid)	Matching Registered Transcripts
NP_000972.1:p.Ala11Ser	CA290376093 NM_000981.4:c.31G>T