Canonical Allele Identifier: PA2826998368
Gene: RARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2165485
ClinVar RCV Id: RCV003084398
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305714.1:p.Ile366Val
CA3916190
NM_001318785.2:c.1096A>G