Canonical Allele Identifier: PA916047485
Gene: ARSL HGNC NCBI

Linked Data

ClinVar Variation Id: 11528
ClinVar RCV Id: RCV000012284
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356009.1:p.Pro603Ser
CA341096
NM_001369080.1:c.1807C>T