Canonical Allele Identifier: PA2825949743
Gene: CERKL HGNC NCBI

Linked Data

ClinVar Variation Id: 1506522
ClinVar RCV Id: RCV002036010
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153749.1:p.Arg228Ser
CA2010671
NM_001160277.2:c.684A>T
CA349740707
NM_001160277.2:c.684A>C