Canonical Allele Identifier: PA2826027077
Gene: S1PR5 HGNC NCBI

Linked Data

ClinVar Variation Id: 788018
ClinVar RCV Id: RCV000970353
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159687.1:p.Leu308His
CA9195799
NM_001166215.2:c.923T>A