Canonical Allele Identifier: PA916060872
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 445293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_942002.1:p.Ser96Arg
CA360196384
NM_198709.3:c.288C>G
CA360196385
NM_198709.3:c.288C>A
CA360196398
NM_198709.3:c.286A>C