Canonical Allele Identifier: PA1139697806
Gene: RPS19 HGNC NCBI

Linked Data

ClinVar Variation Id: 941888
ClinVar RCV Id: RCV001211758 RCV001292964
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308413.1:p.Val87Ile
CA9465358
NM_001321484.1:c.259G>A