Canonical Allele Identifier: PA2828565947
Gene: FARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1052874
ClinVar RCV Id: RCV001361138
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362186.1:p.Thr121Met
CA3623632
NM_001375257.1:c.362C>T