Allele Registry

Canonical Allele Identifier: PA2826661289

Gene: ARSL HGNC NCBI

ClinVar RCV:

RCV000020091

ClinVar Variation:

21032

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269560.2:p.Thr427Met	CA341531 NM_001282631.2:c.1280C>T