Canonical Allele Identifier: PA2825205952
Gene: SMPD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1173987
ClinVar RCV Id: RCV001527442

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000534.3:p.[Pro313Leu;Val314_Tyr315insGlyGlnHisGlyVal]
CA2499221118
NM_000543.5:c.938_939delinsTGGTGGGCCAGCATGGT