Canonical Allele Identifier: PA2827064412
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_001308414.1:p.Phe63Ser
CA406029809
NM_001321485.1:c.188T>C
CA915951693
NM_001321485.1:c.188_189delinsCT