Canonical Allele Identifier: PA916013596
Gene: ARSL HGNC NCBI

Linked Data

ClinVar Variation Id: 427005
ClinVar RCV Id: RCV000489401

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269560.2:p.Arg57Cys
CA412267620
NM_001282631.2:c.169C>T