Canonical Allele Identifier: PA645381253
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 379809
ClinVar RCV Id: RCV000435336 RCV000632186
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000037.2:p.Thr442Met
CA16604916
NM_000046.5:c.1325C>T