Canonical Allele Identifier: PA220289
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 92356
ClinVar RCV Id: RCV000078005 RCV000677616 RCV001266364
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000037.2:p.Gly324Val
CA220288
NM_000046.5:c.971G>T