Canonical Allele Identifier: PA2580318779
Gene: FARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 1717480
ClinVar RCV Id: RCV002296388
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005678.3:p.His565Tyr
CA350805459
NM_005687.5:c.1693C>T