Allele Registry

Canonical Allele Identifier: PA357214

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV000210597

ClinVar Variation:

224973

HGVS (amino-acid)	Matching Registered Transcripts
NP_000039.2:p.Leu154Pro	CA357213 NM_000048.4:c.461T>C