Canonical Allele Identifier: PA2828309892
Gene: ARSL HGNC NCBI

Linked Data

ClinVar Variation Id: 11522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356008.1:p.Arg21Ser
CA255919
NM_001369079.1:c.63G>C
CA412268778
NM_001369079.1:c.63G>T