Canonical Allele Identifier: PA2826978504
Gene: SMPD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 93311
ClinVar Variation Id: 1090434
ClinVar RCV Id: RCV001409612

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305016.1:p.Val36Ala
CA146857
NM_001318087.2:c.107T>C
CA2499221113
NM_001318087.2:c.107_108delinsCT