Canonical Allele Identifier: PA645381237
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 430162
ClinVar RCV Id: RCV000493516 RCV000677613
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000037.2:p.Ser320Arg
CA360343325
NM_000046.5:c.960C>A
CA360343328
NM_000046.5:c.960C>G
CA360343339
NM_000046.5:c.958A>C