Canonical Allele Identifier: PA091629
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 643476
ClinVar RCV Id: RCV000797180 RCV001759511
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000039.2:p.Arg126Trp
CA159927114
NM_000048.4:c.376C>T