Canonical Allele Identifier: PA2826978731
Gene: SMPD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2139959
ClinVar RCV Id: RCV003052871
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305016.1:p.Leu256Pro
CA5852682
NM_001318087.2:c.767T>C