Canonical Allele Identifier: PA916057356
Gene: S1PR5 HGNC NCBI

Linked Data

ClinVar Variation Id: 788018
ClinVar RCV Id: RCV000970353

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110387.1:p.Leu308His
CA9195799
NM_030760.5:c.923T>A