Canonical Allele Identifier: PA2828565970
Gene: FARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 253159
ClinVar RCV Id: RCV000239526
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362186.1:p.Asp142Tyr
CA10586223
NM_001375257.1:c.424G>T