Canonical Allele Identifier: PA2825338908
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 2401
ClinVar RCV Id: RCV000002502
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020117.1:p.Arg359Cys
CA339980
NM_001024946.2:c.1075C>T