Canonical Allele Identifier: PA2827111335
Gene: RPS19 HGNC NCBI

Linked Data

ClinVar Variation Id: 3236681
ClinVar RCV Id: RCV004556141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308413.1:p.Asp118Gly
CA406030619
NM_001321484.1:c.353A>G