Canonical Allele Identifier: PA2828565837
Gene: FARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 429663
ClinVar RCV Id: RCV000493622 RCV001250393 RCV002509414 RCV003156098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361808.1:p.Arg419His
CA3623926
NM_001374879.1:c.1256G>A