Canonical Allele Identifier: PA2826978871
Gene: SMPD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2103537
ClinVar RCV Id: RCV003022199

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305016.1:p.Leu382Val
CA379373003
NM_001318087.2:c.1144C>G