Canonical Allele Identifier: PA105758
Gene: ASAH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 92
ClinVar RCV Id: RCV000000112 RCV000853547
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_808592.2:p.Glu138Val
CA113840
NM_177924.5:c.413A>T