Allele Registry

Canonical Allele Identifier: PA2741825991

Gene: ASL HGNC NCBI

ClinVar RCV:

RCV003472630

ClinVar Variation:

2678634

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020114.1:p.Ala444Val	CA4277390 NM_001024943.2:c.1331C>T