Canonical Allele Identifier: PA2499248638
Gene: RPS19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1071332
ClinVar RCV Id: RCV001383782

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308413.1:p.Arg62Pro
CA406029874
NM_001321484.1:c.185G>C