Canonical Allele Identifier: PA2825338862
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_001020117.1:p.Gln300His
CA4277213
NM_001024946.2:c.900G>C
CA367646723
NM_001024946.2:c.900G>T