Canonical Allele Identifier: PA916044109
Gene: ASAH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 180643
ClinVar RCV Id: RCV000157605 RCV000853058 RCV004551355
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350672.1:p.Lys87Asn
CA185930
NM_001363743.1:c.261A>C
CA370431462
NM_001363743.1:c.261A>T