Canonical Allele Identifier: PA2827547690
Gene: RARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 402195
ClinVar RCV Id: RCV000454292 RCV002225614 RCV002282147 RCV002522741 RCV003418144 RCV003463833
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337436.1:p.Ser268Pro
CA3916314
NM_001350507.1:c.802T>C