Canonical Allele Identifier: PA2828566353
Gene: FARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 587677
ClinVar RCV Id: RCV000714948 RCV003326510
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362187.1:p.Thr156Met
CA3623651
NM_001375258.1:c.467C>T