Canonical Allele Identifier: PA2826661297
Gene: ARSL HGNC NCBI

Linked Data

ClinVar Variation Id: 11527
ClinVar RCV Id: RCV000012283
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269560.2:p.Cys438Tyr
CA255923
NM_001282631.2:c.1313G>A