Canonical Allele Identifier: PA2826660887
Gene: ARSL HGNC NCBI

Linked Data

ClinVar Variation Id: 1805736
ClinVar RCV Id: RCV002472154

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269557.1:p.Gly169Arg
CA412267414
NM_001282628.2:c.505G>C
CA412267415
NM_001282628.2:c.505G>A