Canonical Allele Identifier: PA2580318728
Gene: FARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 2228575
ClinVar RCV Id: RCV002707776
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005678.3:p.Asp312Asn
CA65827794
NM_005687.5:c.934G>A