Canonical Allele Identifier: PA2828566369
Gene: FARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1449177
ClinVar RCV Id: RCV002004541 RCV002492096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362187.1:p.Leu172Pro
CA3623663
NM_001375258.1:c.515T>C