Canonical Allele Identifier: PA2828169329
Gene: SMPD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1112053
ClinVar RCV Id: RCV001438855

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352064.1:p.Ser367Ala
CA2499221120
NM_001365135.1:c.1099T>G