Canonical Allele Identifier: PA2573247529
Gene: FARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 1511922
ClinVar RCV Id: RCV002016947
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005678.3:p.Ala287Gly
CA2136515
NM_005687.5:c.860C>G