Allele Registry

Canonical Allele Identifier: PA916013591

Gene: ARSL HGNC NCBI

ClinVar Variation Id: 383365

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269560.2:p.Trp8Ser	CA16608880 NM_001282631.2:c.23G>C