Canonical Allele Identifier: PA2826660832
Gene: ARSL HGNC NCBI

Linked Data

ClinVar Variation Id: 11522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269557.1:p.Arg37Ser
CA255919
NM_001282628.2:c.111G>C
CA412268778
NM_001282628.2:c.111G>T