Canonical Allele Identifier: PA2828566338
Gene: FARS2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362187.1:p.Asp142Tyr
CA10586223
NM_001375258.1:c.424G>T