Canonical Allele Identifier: PA2828310184
Gene: ARSL HGNC NCBI

Linked Data

ClinVar Variation Id: 1805736
ClinVar RCV Id: RCV002472154

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356009.1:p.Gly169Arg
CA412267414
NM_001369080.1:c.505G>C
CA412267415
NM_001369080.1:c.505G>A