Canonical Allele Identifier: PA2573070426
Gene: RPS19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1338146
ClinVar RCV Id: RCV001822744
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308414.1:p.Leu100Phe
CA406030465
NM_001321485.1:c.298C>T