Canonical Allele Identifier: PA091587
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 496789

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000037.2:p.Arg152Trp
CA121107804
NM_000046.5:c.454C>T