Canonical Allele Identifier: PA2828108578
Gene: ASAH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1375276
ClinVar RCV Id: RCV001879592
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350672.1:p.Thr188Ser
CA4650690
NM_001363743.1:c.563C>G
CA370429327
NM_001363743.1:c.562A>T