Canonical Allele Identifier: PA2827064543
Gene: RPS19 HGNC NCBI

Linked Data

ClinVar Variation Id: 372495
ClinVar RCV Id: RCV000414046 RCV002323577
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308414.1:p.Arg140Leu
CA16043115
NM_001321485.1:c.419G>T