Canonical Allele Identifier: PA645381174
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 286297

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000037.2:p.Phe62Tyr
CA3318344
NM_000046.5:c.185T>A