Allele Registry

Canonical Allele Identifier: PA111952

Gene: RPL21 HGNC NCBI

ClinVar Allele:

143259

ClinVar RCV:

RCV000128579

ClinVar Variation:

139638

HGVS (amino-acid)	Matching Registered Transcripts
NP_000973.2:p.Arg32Gln	CA163349 NM_000982.4:c.95G>A