Canonical Allele Identifier: PA2826661083
Gene: ARSL HGNC NCBI

Linked Data

ClinVar Variation Id: 11528
ClinVar RCV Id: RCV000012284

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269557.1:p.Pro603Ser
CA341096
NM_001282628.2:c.1807C>T