Canonical Allele Identifier: PA2827055056
Gene: S1PR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2276643
ClinVar RCV Id: RCV004130783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307659.1:p.Ile344Met
CA972781
NM_001320730.2:c.1032C>G