Canonical Allele Identifier: PA2828564887
Gene: FARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1045397
ClinVar RCV Id: RCV001349804
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361806.1:p.His159Gln
CA3623653
NM_001374877.1:c.477C>A
CA362735368
NM_001374877.1:c.477C>G