Canonical Allele Identifier: PA916045078
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_001352064.1:p.Val36Ala
CA146857
NM_001365135.1:c.107T>C
CA2499221113
NM_001365135.1:c.107_108delinsCT