Canonical Allele Identifier: PA916060965
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 496789

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_942002.1:p.Arg152Trp
CA121107804
NM_198709.3:c.454C>T