Canonical Allele Identifier: PA2828168696
Gene: SMPD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3166641
ClinVar RCV Id: RCV004462025
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352064.1:p.Ser52Phe
CA379367630
NM_001365135.1:c.155C>T