Canonical Allele Identifier: PA2829911853
Gene: MRPS22 HGNC NCBI

Linked Data

ClinVar Variation Id: 3209050
ClinVar RCV Id: RCV004504926

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064576.1:p.Leu261Val
CA354763065
NM_020191.4:c.781C>G