Canonical Allele Identifier: PA915957108
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 92366
ClinVar RCV Id: RCV000078016

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020115.1:p.Ser282Arg
CA220294
NM_001024944.2:c.846C>G
CA367645440
NM_001024944.2:c.844A>C
CA367645457
NM_001024944.2:c.846C>A