Canonical Allele Identifier: PA2825338828
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 2399
ClinVar RCV Id: RCV000002500 RCV000078017
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020117.1:p.Gln260Arg
CA252263
NM_001024946.2:c.779A>G