Canonical Allele Identifier: PA2829487847
Gene: S1PR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3157416
ClinVar RCV Id: RCV004447259
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004221.3:p.Met340Leu
CA403945026
NM_004230.4:c.1018A>T
CA403945033
NM_004230.4:c.1018A>C