Canonical Allele Identifier: PA2826978951
Gene: SMPD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1116265
ClinVar RCV Id: RCV001444599

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305017.1:p.Pro19Leu
CA217299749
NM_001318088.2:c.56C>T