Canonical Allele Identifier: PA645442426
Gene: CERKL HGNC NCBI

Linked Data

ClinVar Variation Id: 423197

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001025482.1:p.Gln402Pro
CA2010566
NM_001030311.3:c.1205A>C