Canonical Allele Identifier: PA2826027062
Gene: S1PR5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2400658
ClinVar RCV Id: RCV004238483

Amino-acid Alleles

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