Canonical Allele Identifier: PA220287
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 92355

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000037.2:p.Trp312Arg
CA220286
NM_000046.5:c.934T>C
CA360343429
NM_000046.5:c.934T>A