Canonical Allele Identifier: PA357218
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 224976
ClinVar RCV Id: RCV000210606

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000039.2:p.Ser254Arg
CA357217
NM_000048.4:c.762C>A
CA367645177
NM_000048.4:c.760A>C
CA367645181
NM_000048.4:c.762C>G