Canonical Allele Identifier: PA2825338823
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 427091
ClinVar RCV Id: RCV000489046 RCV000669138
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020117.1:p.Gly254Glu
CA367645418
NM_001024946.2:c.761G>A