Canonical Allele Identifier: PA2825299279
Gene: RPS19 HGNC NCBI

Linked Data

ClinVar Variation Id: 3030171
ClinVar RCV Id: RCV003901375

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001013.1:p.Thr76Ile
CA406030140
NM_001022.3:c.227C>T