Canonical Allele Identifier: PA113290
Gene: RPS19 HGNC NCBI

Linked Data

ClinVar Variation Id: 6320

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001013.1:p.Gly127Glu
CA130769
NM_001022.3:c.380G>A