Allele Registry

Canonical Allele Identifier: PA2828565997

Gene: FARS2 HGNC NCBI

ClinVar RCV:

RCV000200335

RCV000557427

RCV003937732

ClinVar Variation:

214338

HGVS (amino-acid)	Matching Registered Transcripts
NP_001362186.1:p.Asp169Val	CA324892 NM_001375257.1:c.506A>T