Canonical Allele Identifier: PA2825027613
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 2745696
ClinVar RCV Id: RCV003495040

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000037.2:p.Arg160Gly
CA360193896
NM_000046.5:c.478C>G