Allele Registry

Canonical Allele Identifier: PA3057257956

Gene: ARSB HGNC NCBI

ClinVar RCV:

RCV004587790

ClinVar Variation:

3251384

HGVS (amino-acid)	Matching Registered Transcripts
NP_942002.1:p.Val358Leu	CA121690793 NM_198709.3:c.1072G>C CA121690794 NM_198709.3:c.1072G>T