Canonical Allele Identifier: PA105849
Gene: ASAH1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_808592.2:p.Tyr36Cys
CA113842
NM_177924.5:c.107A>G