Canonical Allele Identifier: PA2825299708
Gene: RPS27 HGNC NCBI

Linked Data

ClinVar Variation Id: 3156186
ClinVar RCV Id: RCV004452064
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001021.1:p.Pro12Ser
CA342587043
NM_001030.6:c.34C>T