Canonical Allele Identifier: PA2829991068
Gene: SPHK1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

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