Canonical Allele Identifier: PA2825338363
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 2851810
ClinVar RCV Id: RCV003604919

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020115.1:p.Leu49Met
CA367638261
NM_001024944.2:c.145C>A