Canonical Allele Identifier: PA091678
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 2402
ClinVar RCV Id: RCV000002503 RCV000723377
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000039.2:p.Val178Met
CA252264
NM_000048.4:c.532G>A