Canonical Allele Identifier: PA2825949734
Gene: CERKL HGNC NCBI

Linked Data

ClinVar Variation Id: 636008
ClinVar RCV Id: RCV000787563
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153749.1:p.Gly214Arg
CA61590116
NM_001160277.2:c.640G>A
CA349741073
NM_001160277.2:c.640G>C