Canonical Allele Identifier: PA2826979010
Gene: SMPD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1501508
ClinVar RCV Id: RCV002017523
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305017.1:p.Pro123Ser
CA217301969
NM_001318088.2:c.367C>T