Canonical Allele Identifier: PA2826115081
Gene: RPS27A HGNC NCBI

Linked Data

ClinVar Variation Id: 2275590
ClinVar RCV Id: RCV004130708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001170884.1:p.Ile36Val
CA346903625
NM_001177413.1:c.106A>G