Canonical Allele Identifier: PA233695
Gene: CERKL HGNC NCBI

Linked Data

ClinVar Variation Id: 166850

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_963842.1:p.Glu44Asp
CA233693
NM_201548.5:c.132G>C
CA349744653
NM_201548.5:c.132G>T