Canonical Allele Identifier: PA2825299314
Gene: RPS19 HGNC NCBI

Linked Data

ClinVar Variation Id: 3236681
ClinVar RCV Id: RCV004556141

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001013.1:p.Asp118Gly
CA406030619
NM_001022.3:c.353A>G