Canonical Allele Identifier: PA2825949638
Gene: CERKL HGNC NCBI

Linked Data

ClinVar Variation Id: 333011

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153749.1:p.Arg105Trp
CA2010869
NM_001160277.2:c.313C>T