Canonical Allele Identifier: PA2825804981
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_001136074.1:p.Pro12Ser
CA8785056
NM_001142602.2:c.34C>T