Allele Registry

Canonical Allele Identifier: PA2828565970

Gene: FARS2 HGNC NCBI

ClinVar Allele:

247571

ClinVar RCV:

RCV000239526

ClinVar Variation:

253159

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