Canonical Allele Identifier: PA2825949748
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_001153749.1:p.Thr237Ala
CA61590032
NM_001160277.2:c.709A>G