Canonical Allele Identifier: PA091633
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 933174
ClinVar RCV Id: RCV001201220

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000039.2:p.Arg186Gln
CA4277005
NM_000048.4:c.557G>A