Canonical Allele Identifier: PA2825338187
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 1499842
ClinVar RCV Id: RCV002042436
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020114.1:p.Met230Ile
CA367644657
NM_001024943.2:c.690G>A
CA367644660
NM_001024943.2:c.690G>C
CA367644662
NM_001024943.2:c.690G>T