Canonical Allele Identifier: PA2826978722
Gene: SMPD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 371576
ClinVar Variation Id: 553926
ClinVar RCV Id: RCV000669468

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305016.1:p.Ser250Arg
CA5852678
NM_001318087.2:c.748A>C
CA379370932
NM_001318087.2:c.750C>A
CA379370933
NM_001318087.2:c.750C>G