Canonical Allele Identifier: PA2828108589
Gene: ASAH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1398318

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350672.1:p.Ser197Cys
CA370429239
NM_001363743.1:c.589A>T