Canonical Allele Identifier: PA2580473970
Gene: S1PR5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2400658
ClinVar RCV Id: RCV004238483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110387.1:p.Ala143Thr
CA9195893
NM_030760.5:c.427G>A