Canonical Allele Identifier: PA2825338808
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 224976
ClinVar RCV Id: RCV000210606

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020117.1:p.Ser228Arg
CA357217
NM_001024946.2:c.684C>A
CA367645177
NM_001024946.2:c.682A>C
CA367645181
NM_001024946.2:c.684C>G