Canonical Allele Identifier: PA2828169369
Gene: SMPD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1501508
ClinVar RCV Id: RCV002017523

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352064.1:p.Pro386Ser
CA217301969
NM_001365135.1:c.1156C>T