Canonical Allele Identifier: PA2830369022
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_808592.2:p.Thr253Ser
CA4650690
NM_177924.5:c.758C>G
CA370429327
NM_177924.5:c.757A>T