Canonical Allele Identifier: PA658825577
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 559788
ClinVar RCV Id: RCV000677567
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000037.2:p.His147Pro
CA360194032
NM_000046.5:c.440A>C