Canonical Allele Identifier: PA2828565285
Gene: FARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1019925
ClinVar RCV Id: RCV001319429
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361807.1:p.Ala196Ser
CA3623679
NM_001374878.1:c.586G>T