Canonical Allele Identifier: PA645379645
Gene: ARSL HGNC NCBI

Linked Data

ClinVar Variation Id: 427005
ClinVar RCV Id: RCV000489401
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000038.2:p.Arg111Cys
CA412267620
NM_000047.3:c.331C>T