Canonical Allele Identifier: PA658749848
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 495379
ClinVar RCV Id: RCV000587929 RCV001576060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000039.2:p.Ile100Thr
CA4276893
NM_000048.4:c.299T>C