Canonical Allele Identifier: PA091601
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 879

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000037.2:p.Leu236Pro
CA114602
NM_000046.5:c.707T>C