Allele Registry

Canonical Allele Identifier: PA253775

Gene: RPS26 HGNC NCBI

ClinVar Allele:

21161

ClinVar RCV:

RCV000006496

RCV002415402

RCV003225019

ClinVar Variation:

6122

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020.2:p.Met1Val