Canonical Allele Identifier: PA2825624683
Gene: ASAH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 362377

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120977.1:p.Tyr201Phe
CA4650766
NM_001127505.3:c.602A>T