Canonical Allele Identifier: PA916025060
Gene: RPS19 HGNC NCBI

Linked Data

ClinVar Variation Id: 640546
ClinVar RCV Id: RCV000793592
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308413.1:p.Ser59Leu
CA915951693
NM_001321484.1:c.175_176delinsCT