Canonical Allele Identifier: PA2826027062
Gene: S1PR5 HGNC NCBI
ClinVar RCV:
RCV004238483
ClinVar Variation:
2400658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159687.1:p.Ala143Thr
CA9195893
NM_001166215.2:c.427G>A