Canonical Allele Identifier: PA091626
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_000039.2:p.Ala205Val
CA312324
NM_000048.4:c.614C>T