Canonical Allele Identifier: PA2828566055
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_001362186.1:p.Ala235Val
CA3623715
NM_001375257.1:c.704C>T