Canonical Allele Identifier: PA2828565425
Gene: FARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 214335
ClinVar RCV Id: RCV000200808 RCV000525331 RCV000578164 RCV000622524 RCV003156085
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361807.1:p.Pro361Leu
CA325392
NM_001374878.1:c.1082C>T