Canonical Allele Identifier: PA2825028666
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 966088
ClinVar RCV Id: RCV001240679
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000039.2:p.Ser421Leu
CA4277368
NM_000048.4:c.1262C>T