Canonical Allele Identifier: PA2825338131
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 2402

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020114.1:p.Val178Met
CA252264
NM_001024943.2:c.532G>A