Canonical Allele Identifier: PA658825579
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_000037.2:p.Thr164del
CA560767968
NM_000046.5:c.489_491del