Canonical Allele Identifier: PA2827064510
Gene: RPS19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2063019
ClinVar RCV Id: RCV002958189
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308414.1:p.Gln101Glu
CA9465363
NM_001321485.1:c.301C>G