Canonical Allele Identifier: PA916022230
Gene: SMPD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2992

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305016.1:p.His423Tyr
CA252523
NM_001318087.2:c.1267C>T