Canonical Allele Identifier: PA2825338099
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 3032644
ClinVar RCV Id: RCV003902328
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020114.1:p.Leu136Pro
CA367639385
NM_001024943.2:c.407T>C