Canonical Allele Identifier: PA2825338757
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 203614
ClinVar RCV Id: RCV000634853
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020117.1:p.Ala179Val
CA312324
NM_001024946.2:c.536C>T