Canonical Allele Identifier: PA2825949738
Gene: CERKL HGNC NCBI

Linked Data

ClinVar Variation Id: 2060761
ClinVar RCV Id: RCV002947969

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153749.1:p.Ser219Arg
CA349740962
NM_001160277.2:c.657C>G
CA349740966
NM_001160277.2:c.657C>A
CA349740986
NM_001160277.2:c.655A>C