Canonical Allele Identifier: PA2826661328
Gene: ARSL HGNC NCBI

Linked Data

ClinVar Variation Id: 11528
ClinVar RCV Id: RCV000012284

Amino-acid Alleles

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