Canonical Allele Identifier: PA2827111108
Gene: RPS19 HGNC NCBI

Linked Data

ClinVar Variation Id: 3030171
ClinVar RCV Id: RCV003901375

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308412.1:p.Thr76Ile
CA406030140
NM_001321483.1:c.227C>T