Canonical Allele Identifier: PA2580199020
Gene: SMPD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2131195
ClinVar RCV Id: RCV003061886
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305016.1:p.His427Tyr
CA379374249
NM_001318087.2:c.1279C>T