Canonical Allele Identifier: PA2580121126
Gene: RPS27 HGNC NCBI

Linked Data

ClinVar Variation Id: 2057360
ClinVar RCV Id: RCV002923318 RCV004067137
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001021.1:p.Pro10Leu
CA1123837
NM_001030.6:c.29C>T