Canonical Allele Identifier: PA645483273
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 426324
ClinVar RCV Id: RCV000489610 RCV001836830
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000039.2:p.Gln326His
CA4277213
NM_000048.4:c.978G>C
CA367646723
NM_000048.4:c.978G>T