Canonical Allele Identifier: PA2830462608
Gene: CERKL HGNC NCBI

Linked Data

ClinVar Variation Id: 2121865
ClinVar RCV Id: RCV003043411
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_963842.1:p.Val262Ile
CA349740227
NM_201548.5:c.784G>A