Canonical Allele Identifier: PA2829991068
Gene: SPHK1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2356726
ClinVar RCV Id: RCV004193409
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068807.2:p.Pro26Ser
CA8785056
NM_021972.4:c.76C>T