Canonical Allele Identifier: PA916061014
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 527327

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_942002.1:p.Thr216Ile
CA3318218
NM_198709.3:c.647C>T