Canonical Allele Identifier: PA185931
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_004306.3:p.Lys168Asn
CA185930
NM_004315.6:c.504A>C
CA370431462
NM_004315.6:c.504A>T