Canonical Allele Identifier: PA2828310112
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_001356008.1:p.Cys501Tyr
CA255923
NM_001369079.1:c.1502G>A