Allele Registry

Canonical Allele Identifier: PA916047485

Gene: ARSL HGNC NCBI

ClinVar RCV:

RCV000012284

ClinVar Variation:

11528

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