Canonical Allele Identifier: PA2580133611
Gene: CERKL HGNC NCBI

Linked Data

ClinVar Variation Id: 2439920
ClinVar RCV Id: RCV003144820

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001025482.1:p.Leu296Val
CA349740103
NM_001030311.3:c.886T>G