Canonical Allele Identifier: PA105806
Gene: ASAH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 180643

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_808592.2:p.Lys152Asn
CA185930
NM_177924.5:c.456A>C
CA370431462
NM_177924.5:c.456A>T