Canonical Allele Identifier: PA2573210787
Gene: FARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1427586
ClinVar RCV Id: RCV001945956
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362189.1:p.Ala3Val
CA3623715
NM_001375260.1:c.8C>T