Canonical Allele Identifier: PA2825299308
Gene: RPS19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2120810
ClinVar RCV Id: RCV003025316
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001013.1:p.Leu110Val
CA406030554
NM_001022.3:c.328C>G