Canonical Allele Identifier: PA2573177978
Gene: CERKL HGNC NCBI

Linked Data

ClinVar Variation Id: 1516196
ClinVar RCV Id: RCV002023772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001025482.1:p.Thr281Ala
CA61590032
NM_001030311.3:c.841A>G