Canonical Allele Identifier: PA645379627
Gene: ARSL HGNC NCBI

Linked Data

ClinVar Variation Id: 383365
ClinVar RCV Id: RCV000435946 RCV001824764 RCV002230039
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000038.2:p.Cys8Ser
CA16608880
NM_000047.3:c.23G>C
CA412269745
NM_000047.3:c.22T>A