Canonical Allele Identifier: PA2825949732
Gene: CERKL HGNC NCBI

Linked Data

ClinVar Variation Id: 2813457
ClinVar RCV Id: RCV003678012
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153749.1:p.Gly213Arg
CA349741090
NM_001160277.2:c.637G>C