Canonical Allele Identifier: PA2827111097
Gene: RPS19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1800525
ClinVar RCV Id: RCV002461664
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308412.1:p.Arg67Pro
CA406029967
NM_001321483.1:c.200G>C