Allele Registry

Canonical Allele Identifier: PA645483279

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV000211672

ClinVar Variation:

226414

HGVS (amino-acid)	Matching Registered Transcripts
NP_000039.2:p.Met360Thr	CA10576340 NM_000048.4:c.1079T>C