Canonical Allele Identifier: PA658800732
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 445293
ClinVar RCV Id: RCV000656131 RCV001584227
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000037.2:p.Ser96Arg
CA360196384
NM_000046.5:c.288C>G
CA360196385
NM_000046.5:c.288C>A
CA360196398
NM_000046.5:c.286A>C