Canonical Allele Identifier: PA2827023088
Gene: FARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1389745
ClinVar RCV Id: RCV001898052
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305801.1:p.Glu394Gly
CA362736999
NM_001318872.2:c.1181A>G