Canonical Allele Identifier: PA891866110
Gene: RPS19 HGNC NCBI

Linked Data

ClinVar Variation Id: 6316
ClinVar RCV Id: RCV000033185
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308414.1:p.Glu88Val
CA130766
NM_001321485.1:c.263A>T