Allele Registry

Canonical Allele Identifier: PA2826661043

Gene: ARSL HGNC NCBI

ClinVar RCV:

RCV000020091

ClinVar Variation:

21032

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269557.1:p.Thr506Met	CA341531 NM_001282628.2:c.1517C>T