Canonical Allele Identifier: PA2828565627
Gene: FARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 473311
ClinVar RCV Id: RCV000546306 RCV002483484 RCV003222035
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361808.1:p.Ala166Val
CA3623658
NM_001374879.1:c.497C>T