Canonical Allele Identifier: PA2827548521
Gene: RARS2 HGNC NCBI
ClinVar RCV:
RCV003084398
ClinVar Variation:
2165485
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337439.1:p.Ile366Val
CA3916190
NM_001350510.2:c.1096A>G