Canonical Allele Identifier: PA2825949564
Gene: CERKL HGNC NCBI

Linked Data

ClinVar Variation Id: 166850
ClinVar RCV Id: RCV000415943 RCV001138253
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153749.1:p.Glu44Asp
CA233693
NM_001160277.2:c.132G>C
CA349744653
NM_001160277.2:c.132G>T