Canonical Allele Identifier: PA2825949940
Gene: CERKL HGNC NCBI

Linked Data

ClinVar Variation Id: 166843

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153749.1:p.Ser490Leu
CA233684
NM_001160277.2:c.1469C>T