Canonical Allele Identifier: PA658825569
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 559777
ClinVar RCV Id: RCV000677555
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000037.2:p.Pro130Leu
CA360194254
NM_000046.5:c.389C>T