Canonical Allele Identifier: PA2825299307
Gene: RPS19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1728922
ClinVar RCV Id: RCV002324585
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001013.1:p.Leu107Pro
CA406030536
NM_001022.3:c.320T>C