Canonical Allele Identifier: PA2741858583
Gene: RPS19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2749277
ClinVar RCV Id: RCV003506958
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308414.1:p.Pro106Ser
CA9465365
NM_001321485.1:c.316C>T