Canonical Allele Identifier: PA658831399
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 427091
ClinVar RCV Id: RCV000489046 RCV000669138
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020114.1:p.Gly280Glu
CA367645418
NM_001024943.2:c.839G>A