Canonical Allele Identifier: PA916060970
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 559790
ClinVar RCV Id: RCV000677569
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_942002.1:p.Thr164del
CA560767968
NM_198709.3:c.489_491del