Allele Registry

Canonical Allele Identifier: PA2826661328

Gene: ARSL HGNC NCBI

ClinVar RCV:

RCV000012284

ClinVar Variation:

11528

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269560.2:p.Pro524Ser	CA341096 NM_001282631.2:c.1570C>T