Canonical Allele Identifier: PA2827064526
Gene: RPS19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2120810
ClinVar RCV Id: RCV003025316

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308414.1:p.Ala114Gly
CA406030554
NM_001321485.1:c.341C>G