Canonical Allele Identifier: PA2826661052
Gene: ARSL HGNC NCBI

Linked Data

ClinVar Variation Id: 11527
ClinVar RCV Id: RCV000012283

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269557.1:p.Cys517Tyr
CA255923
NM_001282628.2:c.1550G>A