Canonical Allele Identifier: PA290846
Gene: FARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 137292
ClinVar RCV Id: RCV000124983 RCV000677020 RCV000714927 RCV001701760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006558.1:p.Asn280Ser
CA290845
NM_006567.5:c.839A>G